Rna metabolism proteins

ABSTRACT

The invention provides human RNA metabolism proteins (RMEP) and polynucleotides which identify and encode RMEP. The invention also provides expression vectors, host cells, antibodies, agonists, and antagonists. The invention also provides methods for diagnosing, treating, or preventing disorders associated with aberrant expression of RMEP.

TECHNICAL FIELD

[0001] This invention relates to nucleic acid and amino acid sequences of RNA metabolism proteins and to the use of these sequences in the diagnosis, treatment, and prevention of nervous system, autoimmune/inflammatory, cell proliferative, and developmental disorders, and in the assessment of the effects of exogenous compounds on the expression of nucleic acid and amino acid sequences of RNA metabolism proteins.

BACKGROUND OF THE INVENTION

[0002] Ribonucleic acid (RNA) is a linear single-stranded polymer of four nucleotides, ATP, CTP, UTP, and GTP. In most organisms, RNA is transcribed as a copy of deoxyribonucleic acid (DNA), the genetic material of the organism. In retroviruses RNA rather than DNA serves as the genetic material. RNA copies of the genetic material encode proteins or serve various structural, catalytic, or regulatory roles in organisms. RNA is classified according to its cellular localization and function. Messenger RNAs (mRNAs) encode polypeptides. Ribosomal RNAs (rRNAs) are assembled, along with ribosomal proteins, into ribosomes, which are cytoplasmic particles that translate mRNA into polypeptides. Transfer RNAs (tRNAs) are cytosolic adaptor molecules that function in mRNA translation by recognizing both an mRNA codon and the amino acid that matches that codon. Heterogeneous nuclear RNAs (hnRNAs) include mRNA precursors and other nuclear RNAs of various sizes. Small nuclear RNAs (snRNAs) are a part of the nuclear spliceosome complex that removes intervening, non-coding sequences (introns) and rejoins exons in pre-mRNAs.

[0003] Proteins are associated with RNA during its transcription from DNA, RNA processing, and translation of mRNA into protein. Proteins are also associated with RNA as it is used for structural, catalytic, and regulatory purposes.

[0004] RNA Processing

[0005] Various proteins are necessary for processing of transcribed RNAs in the nucleus. Pre-mRNA processing steps include capping at the 5′ end with methylguanosine, polyadenylating the 3′ end, and splicing to remove introns. The spliceosomal complex is comprised of five small nuclear ribonucleoprotein particles (snRNPs) designated U1, U2, U4, U5, and U6. Each snRNP contains a single species of snRNA and about ten proteins. The RNA components of some snRNPs recognize and base-pair with intron consensus sequences. The protein components mediate spliceosome assembly and the splicing reaction.

[0006] An early step in pre-mRNA cleavage involves the cleavage factor Im (CF hm). The human CF Im protein aids in the recruitment and assembly of processing factors that make up the 3′ end processing complex (Ruegsegger, U. et al (1998) Mol. Cell. 1:243-253). The murine formin binding proteins (FBP's) FBP11 and FBP12 are components of pre-mRNA splicing complexes that facilitate the bridging of 5′ and 3′ ends of the intron. These proteins function through bridging interactions invloving U1 and U2 snRNPs. Autoantibodies to snRNP proteins are found in the blood of patients with systemic lupus erythematosus (Stryer, L. (1995) Biochemistry W. H. Freeman and Company, New York N.Y., p. 863).

[0007] Heterogeneous nuclear ribonucleoproteins (hnRNPs) have been identified that have roles in splicing, exporting of the mature RNAs to the cytoplasm, and mRNA translation (Biamonti, G. et al. (1998) Clin. Exp. Rheumatol. 16:317-326). Some examples of hnRNPs include the yeast proteins Hrp1p, involved in cleavage and polyadenylation at the 3′ end of the RNA; Cbp80p, involved in capping the 5′ end of the RNA; and Np13p, a homolog of mammalian hnRNP A1, involved in export of mRNA from the nucleus (Shen, E. C. et al. (1998) Genes Dev. 12:679-691). HnRNPs have been shown to be important targets of the autoimmune response in rheumatic diseases (Biamonti, supra).

[0008] Many snRNP and hnRNP proteins are characterized by an RNA recognition motif (RRM). (Reviewed in Birney, E. et al. (1993) Nucleic Acids Res. 21:5803-5816.) The RRM is about 80 amino acids in length and forms four β-strands and two α-helices arranged in an α/β sandwich. The RRM contains a core RNP-1 octapeptide motif along with surrounding conserved sequences. In addition to snRNP proteins, examples of RNA-binding proteins which contain the above motifs include heteronuclear ribonucleoproteins which stabilize nascent RNA and factors which regulate alternative splicing. Alternative splicing factors include developmentally regulated proteins, specific examples of which have been identified in lower eukaryotes such as Drosophila melanogaster and Caenorhabditis elegans. These proteins play key roles in developmental processes such as pattern formation and sex determination, respectively. (See, for example, Hodgkin, J. et al. (1994) Development 120:3681-3689.)

[0009] RNA Stability and Degradation

[0010] RNA helicases alter and regulate RNA conformation and secondary structure by using energy derived from ATP hydrolysis to destabilize and unwind RNA duplexes. The most well-characterized and ubiquitous family of RNA helicases is the DEAD-box family, so named for the conserved B-type ATP-binding motif which is diagnostic of proteins in this family. Over 40 DEAD-box helicases have been identified in organisms as diverse as bacteria, insects, yeast, amphibians, mammals, and plants. DEAD-box helicases function in diverse processes such as translation initiation, splicing, ribosome assembly, and RNA editing, transport, and stability. Some DEAD-box helicases play tissue- and stage-specific roles in spermatogenesis and embryogenesis. All DEAD-box helicases contain several conserved sequence motifs spread out over about 420 amino acids. These motifs include an A-type ATP binding motif, the DEAD-box/B-type ATP-binding motif, a serine/arginine/threonine tripeptide of unknown function, and a C-terminal glycine-rich motif with a possible role in substrate binding and unwinding. In addition, alignment of divergent DEAD-box helicase sequences has shown that 37 amino acid residues are identical among these sequences, suggesting that conservation of these residues is important for helicase function. (Reviewed in Linder, P. et al. (1989) Nature 337:121-122.)

[0011] Overexpression of the DEAD-box 1 protein (DDX1) may play a role in the progression of neuroblastoma (Nb) and retinoblastoma (Rb) tumors. These observations suggest that DDX1 may promote or enhance tumor progression by altering the normal secondary structure and expression levels of RNA in cancer cells. Other DEAD-box helicases have been implicated either directly or indirectly in ultraviolet light-induced tumors, B-cell lymphoma, and myeloid malignancies. (Reviewed in Godbout, R. et al. (1998) J. Biol. Chem. 273:21161-21168.)

[0012] Ribonucleases (RNases) catalyze the hydrolysis of phosphodiester bonds in RNA chains, thus cleaving the RNA. For example, RNase P is a ribonucleoprotein enzyme which cleaves the 5′ end of pre-tRNAs as part of their maturation process. RNase H digests the RNA strand of an RNA/DNA hybrid. Such hybrids occur in cells invaded by retroviruses, and RNase H is an important enzyme in the retroviral replication cycle. RNase H domains are often found as a domain associated with reverse transcriptases. RNase activity in serum and cell extracts is elevated in a variety of cancers and infectious diseases (Schein, C. H. (1997) Nat. Biotechnol. 15:529-536). Regulation of RNase activity is being investigated as a means to control tumor angiogenesis, allergic reactions, viral infection and replication, and fungal infections.

[0013] Degradation of mRNAs having premature termination or nonsense codons is accomplished through a surveillance mechanism that has been termed nonsense-mediated mRNA decay (NMD). This mechanism helps eliminate flawed mRNAs that might code for nonfunctional or deleterious polypeptides. Various NMD components are linked to both yeast and human RNA metabolism disorders (Hentze, M. and Kulozik, A. (1999) Cell 96:307-310).

Translation

[0014] Ribosomal RNAs (rRNAs) are assembled, along with ribosomal proteins, into ribosomes, which are cytoplasmic particles that translate messenger RNA (mRNA) into polypeptides. The eukaryotic ribosome is composed of a 60S (large) subunit and a 40S (small) subunit, which together form the 80S ribosome. In addition to the 18S, 28S, 5S, and 5.8S rRNAs, ribosomes contain from 50 to over 80 different ribosomal proteins, depending on the organism. Ribosomal proteins are classified according to which subunit they belong (i.e., L, if associated with the large 60S large subunit or S if associated with the small 40S subunit). E. coli ribosomes have been the most thoroughly studied and contain 50 proteins, many of which are conserved in all life forms. The structures of nine ribosomal proteins have been solved to less than 3.0Å resolution (i.e., S5, S6, S17, L1, L6, L9, L12, L14, L30), revealing common motifs, such as β-α-β protein folds in addition to acidic and basic RNA-binding motifs positioned between β-strands. Most ribosomal proteins are believed to contact rRNA directly (reviewed in Liljas, A. and Garber, M. (1995) Curr. Opin. Struct Biol. 5:721-727, see also Woodson, S. A. and Leontis, N. B. (1998) Curr. Opin. Struct. Biol. 8:294300; Ramakrishnan, V. and White, S. W. (1998) Trends Biochem. Sci. 23:208-212.)

[0015] Ribosomal proteins may undergo post-translational modifications or interact with other ribosome-associated proteins to regulate translation. For example, the highly homologous 40S ribosomal protein S6 kinases (S6K1 and S6K2) play a key role in the regulation of cell growth by controlling the biosynthesis of translational components which make up the protein synthetic apparatus (including the ribosomal proteins). In the case of S6K1, at least eight phosphorylation sites are believed to mediate kinase activation in a hierarchical fashion (Dufner and Thomas (1999) Exp. Cell. Res. 253:100-109). Some of the ribosomal proteins, including L1, also function as translational repressors by binding to polycistronic mRNAs encoding ribosomal proteins (reviewed in Liljas, A. supra and Garber, N supra).

[0016] Recent evidence suggests that a number of ribosomal proteins have secondary functions independent of their involvement in protein biosynthesis. These proteins function as regulators of cell proliferation and, in some instances, as inducers of cell death. For example, the expression of human ribosomal protein L13a has been shown to induce apoptosis by arresting cell growth in the G2/M phase of the cell cycle. Inhibition of expression of L13a induces apoptosis in target cells, which suggests that this protein is necessary, in the appropriate amount, for cell survival. Similar results have been obtained in yeast where inactivation of yeast homologues of L13a, rp22 and rp23, results in severe growth retardation and death. A closely related ribosomal protein, L7, arrests cells in G1 and also induces apoptosis. Thus, it appears that a subset of ribosomal proteins may function as cell cycle checkpoints and compose a new family of cell proliferation regulators.

[0017] Mapping of individual ribosomal proteins on the surface of intact ribosomes is accomplished using 3D immunocryoelectronmicroscopy, whereby antibodies raised against specific ribosomal proteins are visualized. Progress has been made toward the mapping of L1, L7, and L12 while the structure of the intact ribosome has been solved to only 20-25Å resolution and inconsistencies exist among different crude structures (Frank, J. (1997) Curr. Opin. Struct Biol. 7:266-272).

[0018] Three distinct sites have been identified on the ribosome. The aminoacyl-tRNA acceptor site (A site) receives charged tRNAs (with the exception of the initiator-tRNA). The peptidyl-tRNA site (P site) binds the nascent polypeptide as the amino acid from the A site is added to the elongating chain. Deacylated tRNAs bind in the exit site (E site) prior to their release from the ribosome. The structure of the ribosome is reviewed in Stryer, L. (1995) Biochemistry W. H. Freeman and Company, New York N.Y. pp. 888-9081; Lodish, H. et al. (1995) Molecular Cell Biology Scientific American Books, New York N.Y. pp. 119-138; and Lewin, B (1997) Genes VI Oxford University Press, Inc. New York, N.Y.).

[0019] tRNA Charging

[0020] Correct translation of the genetic code depends upon each amino acid forming a linkage with the appropriate transfer RNA (tRNA). The aminoacyl-tRNA synthetases (aaRSs) are essential proteins found in all living organisms. The aaRSs are responsible for the activation and correct attachment of an amino acid with its cognate tRNA, as the first step in protein biosynthesis. Prokaryotic organisms have at least twenty different types of aaRSs, one for each different amino acid, while eukaryotes usually have two aaRSs, a cytosolic form and a initochondrial form for each different amino acid. The 20 aaRS enzymes can be divided into two structural classes. Class I enzymes add amino acids to the 2′ hydroxyl at the 3′ end of tRNAs while Class II enzymes add amino acids to the 3′ hydroxyl at the 3′ end of tRNAs. Each class is characterized by a distinctive topology of the catalytic domain. Class I enzymes contain a catalytic domain based on the nucleotide-binding ‘Rossman fold’. In particular, a consensus tetrapeptide motif is highly conserved (Prosite Document PDOC00161, Aminoacyl-transfer RNA synthetases class-I signature). Class II enzymes contain a central catalytic domain, which consists of a seven-stranded antiparallel β-sheet domain, as well as N- and C-terminal regulatory domains. Class II enzymes are separated into two groups based on the heterodimeric or homodimeric structure of the enzyme; the latter group is further subdivided by the structure of the N- and C-terminal regulatory domains (Hartlein, M. and Cusack, S. (1995) J. Mol. Evol. 40:519-530). The different aaRSs are believed to be the result of divergent evolution, likely following gene duplication events. Notably, amino acids such as Gln, were among the last to appear in nature and evolutionary studies suggest that Gln-RSs appeared first in eukaryotes and were later horizontally transferred to prokaryotes (Lamour, V. et al. (1994) Proc. Natl. Acad. Sci. U.S.A. 91:867074 and Siatecka, M. et al. (1998) Eur. J. Biochem 256:80-7). The importance of Gln-RS and Gln-tRNA^(Gln) are discussed below.

[0021] In addition to their function in protein synthesis, specific aminoacyl tRNA synthetases also play roles in cellular fidelity, RNA splicing, RNA trafficking, apoptosis, and transcriptional and translational regulation. For example, human tyrosyl-tRNA synthetase can be proteolytically cleaved into two fragments with distinct cytokine activities. The carboxy-terminal domain exhibits monocyte and leukocyte chemotaxis activity as well as stimulating production of myeloperoxidase, tumor necrosis factor-α, and tissue factor. The N-terminal domain binds to the interleukin-8 type A receptor and functions as an interleukin-8-like cytokine. Human tyrosyl-tRNA synthetase is secreted from apoptotic tumor cells and may accelerate apoptosis (Wakasugi, K. and Schimmel, P. (1999) Science 284:147-151). Mitochondrial Neurospora crassa TyrRS and S. cerevisiae LeuRS are essential factors for certain group I intron splicing activities, and human mitochondrial LeuRS can substitute for the yeast LeuRS in a yeast null strain. Certain bacterial aaRSs are involved in regulating their own transcription or translation (Martinis, supra). Several aaRSs are able to synthesize diadenosine oligophosphates, a class of signalling molecules with roles in cell proliferation, differentiation, and apoptosis (Kisselev, L. L. et al. (1998) FEBS Lett 427:157-163; Vartanian, A. et al. (1999) FEBS Lett 456:175-180).

[0022] Under optimal conditions, polypeptide synthesis proceeds at a rate of approximately 40 amino acid residues per second. The rate of misincorporation during translation in on the order of 10⁻⁴ and is primarily the result of aminoacyl-t-RNAs being charged with the incorrect amino acid. Incorrectly charged tRNA are toxic to cells as they result in the incorporation of incorrect amino acid residues into an elongating polypeptide. The rate of translation is presumed to be a compromise between the optimal rate of elongation and the need for translational fidelity. Mathematical calculations predict that 10⁻⁴ is indeed the maximum acceptable error rate for protein synthesis in a biological system (reviewed in Stryer, L. supra and Watson, J. et al. (1987) The Benjamin/Cummings Publishing Co., Inc. Menlo Park, CA). A particularly error prone aminoacyl-tRNA charging event, the charging of tRNA^(Gln) with Gln. A mechanism exist for the correction of this mischarging event which likely has its origins in evolution. Gln was among the last of the 20 naturally occurring amino acids used polypeptide synthesis to appear in nature. Gram positive eubacteria, cyanobacteria, Archeae, and eukaryotic organelles posses a noncanonical pathway for the synthesis of Gln-tRNA^(Gln) based on the transformation of Glu-tRNA^(Gln) (synthesized by Glu-tRNA synthetase, GluRS) using the enzyme Glu-tRNA^(Gln) amidotransferase (Glu-AdT). The reactions involved in the transamidation pathway are as follows (Curnow, A. W. et al. (1997) Nucleic Acids Symposium 36:2-4): $\begin{matrix} {{\overset{GluRS}{{t{RNA}}^{Gln}} + {Glu} + {ATP}}->{{{Glu}\text{-}{t{RNA}}^{Gln}} + {AMP} + {PP}_{i}}} & (1) \\ {{{{Glu}\text{-}\overset{{Glu} - {AdT}}{{t{RNA}}^{Gln}}} + {Gln} + {ATP}}->{{{Gln}\text{-}{tRNA}^{Gln}} + {Glu} + {ADP} + P}} & (2) \end{matrix}$

[0023] A similar enzyme, Asp-tRNA^(Asn) amidotransferase, exists in Archaea, which transforms Asp-tRNA^(Asn) to Asn-tRNA^(Asn). Formylase, the enzyme that transforms Met-tRNA^(fMet) to fMet-tRNA^(fMet) in eubacteria, is likely to be a related enzyme. A hydrolytic activity has also been identified that destroys mischarged Val-tRNA^(Ile) (Schimmel, P. et al. (1998) FASEB J. 12:1599-1609). I likely scenario for the evolution of Glu-AdT in primitive life forms is the absence a specific glutaminyl-tRNA synthetase (GInRS), requiring an alternative pathway for the synthesis of Gln-tRNA^(Gln). In fact, deletion of the Glu-AdT operon in Gram positive bacteria is lethal (Curnow, A. W. et al. (1997) Proc. Natl. Acad Sci. U.S.A. 94:11819-11826). The existence of GluRS activity in other organisms has been inferred by the high degree of conservation in translation machinery in nature; however, GluRS has not been identified in all organisms, including Homo sapiens. Such an enzyme would be responsible for ensuring translational fidelity and reducing the synthesis of defective polypeptides.

[0024] Autoantibodies against aminoacyl-tRNAs are generated by patients with autoimmune diseases such as rheumatic arthritis, dermatomyositis and polymyositis, and correlate strongly with complicating interstitial lung disease (ILD) (Freist, W. et al. (1999) Biol. Chem. 380:623-646; Freist, W. et al. (1996) Biol. Chem. Hoppe Seyler 377:343-356). These antibodies appear to be generated in response to viral infection, and coxsackie virus has been used to induce experimental viral myositis in animals.

[0025] Comparison of aaRS structures between humans and pathogens has been useful in the design of novel antibiotics (Schiramel, sra). Genetically engineered aaRSs have been utilized to allow site-specific incorporation of unnatural amino acids into proteins in vivo (iu, D. R. et al. (1997) Proc. Natl. Acad. Sci. USA 94:10092-10097).

[0026] Translation Initiation

[0027] Initiation of translation can be divided into three stages. The first stage brings an initiator transfer RNA (Met-tRNA_(f)) together with the 40S ribosomal subunit to form the 43S preinitiation complex. The second stage binds the 43S preinitiation complex to the mRNA, followed by migration of the complex to the correct AUG initiation codon. The third stage brings the 60S ribosomal subunit to the 40S subunit to generate an 80S ribosome at the inititation codon. Regulation of translation primarily involves the first and second stage in the initiation process (V. M. Pain (1996) Eur. J. Biochem. 236:747-771).

[0028] Several initiation factors, many of which contain multiple subunits, are involved in bringing an initiator tRNA and 40S ribosomal subunit together. One eukaryotic initiation factor (EIF) EIF5A is an 18-kD protein containing the unique amino acid residue, hypusine (N epsilon-(4-amino-2-hydroxybutyl)lysine) (Rinaudo, M. et al. (1993) Gene 137:303-307). eIF2, a guanine nucleotide binding protein, recruits the initiator tRNA to the 40S ribosomal subunit. Only when eIF2 is bound to GTP does it associate with the initiator tRNA. eIF2B, a guanine nucleotide exchange protein, is responsible for converting eIF2 from the GDP-bound inactive form to the GTP-bound active form. Two other factors, elF1A and eIF3 bind and stabilize the 40S subunit by interacting with 18S ribosomal RNA and specific ribosomal structural proteins. eIF3 is also involved in association of the 40S ribosomal subunit with mRNA. The Met-tRNA_(f), eIF1A, eIF3, and 40S ribosomal subunit together make up the 43S preinitiation complex (Pain, supra).

[0029] Additional factors are required for binding of the 43S preinitiation complex to an mRNA molecule, and the process is regulated at several levels. eIF4F is a complex consisting of three proteins: eIF4E, eIF4A, and eIF4G. eIF4E recognizes and binds to the mRNA 5′-terminal m⁷GTP cap, eIF4A is a bidirectional RNA-dependent helicase, and eIF4G is a scaffolding polypeptide. eIF4G has three binding domains. The N-terminal third of eIF4G interacts with eIF4E, the central third interacts with eIF4A, and the C-terminal third interacts with eIF3 bound to the 43S preinitiation complex. Thus, eIF4G acts as a bridge between the 40S ribosomal subunit and the mRNA (M.W. Hentze (1997) Science 275:500-501).

[0030] The ability of eIF4F to initiate binding of the 43S preinitiation complex is regulated by structural features of the mRNA. The mRNA molecule has an untranslated region (UTR) between the 5′ cap and the AUG start codon. In some mRNAs this region forms secondary structures that impede binding of the 43S preinitiation complex. The helicase activity of eIF4A is thought to function in removing this secondary structure to facilitate binding of the 43S preinitiation complex (Pain, supra).

[0031] Translation Elongation

[0032] Elongation is the process whereby additional amino acids are joined to the initiator methionine to form the complete polypeptide chain. The elongation factors EF1α, EF1β γ, and EF2 are involved in elongating the polypeptide chain following initiation. EF1α is a GTP-binding protein. In EF1α's GTP-bound form, it brings an aminoacyl-tRNA to the ribosome's A site. The amino acid attached to the newly arrived aminoacyl-tRNA forms a peptide bond with the initiatior methionine. The GTP on EF1α is hydrolyzed to GDP, and EF1α-GDP dissociates from the ribosome. EF1β γ binds EF1α-GDP and induces the dissociation of GDP from EF1α, allowing EF1α to bind GTP and a new cycle to begin.

[0033] As subsequent aminoacyl-tRNAs are brought to the ribosome, EF-G, another GTP-binding protein, catalyzes the translocation of tRNAs from the A site to the P site and finally to the E site of the ribosome. This allows the processivity of translation.

[0034] Translation Termination

[0035] The release factor eRF carries out termination of translation. eRF recognizes stop codons in the mRNA, leading to the release of the polypeptide chain from the ribosome.

[0036] The discovery of new RNA metabolism proteins and the polynucleotides encoding them satisfies a need in the art by providing new compositions which are useful in the diagnosis, prevention, and treatment of nervous system, autoimmune/inflammatory, cell proliferative, and developmental disorders, and in the assessment of the effects of exogenous compounds on the expression of nucleic acid and amino acid sequences of RNA metabolism proteins. nervous system disorders, autoimmune/inflammatory disorders, and cell proliferative disorders including cancer

SUMMARY OF THE INVENTION

[0037] The invention features purified polypeptides, RNA metabolism proteins, referred to collectively as “RMEP” and individually as “RMEP-1,” “RMEP-2,” “RMEP-3,” “RMEP-4,” “RMEP-5,” “RMEP-6,” “RMEP-7,” “RMEP-8,” “RMEP-9,” “RMEP-10,” “RMEP-11,” “RMEP-12,” “RMEP-13,” “RMEP-14,” “RMEP-15,” “RMEP-16,” “RMEP-17,” “RMEP-18,” “RMEP-19,” “RMEP-20,” “RMEP-21,” “RMEP-22,” “RMEP-23,” “RMEP-24,” “RMEP-25,” “RMEP-26,” “RMEP-27,” “RMEP-28,” “RMEP-29,” “RMEP-30,” “RMEP-31,” “RMEP-32,” “RMEP-33,” “RMEP-34,” “RMEP-35,” “RMEP-36,” “RMEP-37,” “RMEP-38,” “RMEP-39,” “RMEP-40,” “RMEP-41,” “RMEP-42,” “RMEP-43,” “RMEP-44,” “RMEP-45,” “RMEP-46,” “RMEP-47.” In one aspect, the invention provides an isolated polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, b) a naturally occurring polypeptide comprising an amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47. In one alternative, the invention provides an isolated polypeptide comprising the amino acid sequence of SEQ ID NO:1-47.

[0038] The invention further provides an isolated polynucleotide encoding a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, b) a naturally occurring polypeptide comprising an amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of-SEQ ID NO:1-47, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47. In one alternative, the polynucleotide encodes a polypeptide selected from the group consisting of SEQ ID NO:1-47. In another alternative, the polynucleotide is selected from the group consisting of SEQ ID NO:48-94;

[0039] Additionally, the invention provides a recombinant polynucleotide comprising a promoter sequence operably linked to a polynucleotide encoding a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, b) a naturally occurring polypeptide comprising an amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47. In one alternative, the invention provides a cell transformed with the recombinant polynucleotide. In another alternative, the invention provides a transgenic organism comprising the recombinant polynucleotide.

[0040] The invention also provides a method for producing a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, b) a naturally occurring polypeptide comprising an amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47. The method comprises a) culturing a cell under conditions suitable for expression of the polypeptide, wherein said cell is transformed with a recombinant polynucleotide comprising a promoter sequence operably linked to a polynucleotide encoding the polypeptide, and b) recovering the polypeptide so expressed

[0041] Additionally, the invention provides an isolated antibody which specifically binds to a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, b) a naturally occurring polypeptide comprising an amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47.

[0042] The invention further provides an isolated polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:48-94, b) a naturally occurring polynucleotide comprising a polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:48-94, c) a polynucleotide complementary to the polynucleotide of a), d) a polynucleotide complementary to the polynucleotide of b), and e) an RNA equivalent of a)-d). In one alternative, the polynucleotide comprises at least 60 contiguous nucleotides.

[0043] Additionally, the invention provides a method for detecting a target polynucleotide in a sample, said target polynucleotide having a sequence of a polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:48-94, b) a naturally occurring polynucleotide comprising a polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:48-94, c) a polynucleotide complementary to the polynucleotide of a), d) a polynucleotide complementary to the polynucleotide of b), and e) an RNA equivalent of a)-d). The method comprises a) hybridizing the sample with a probe comprising at least 20 contiguous nucleotides comprising a sequence complementary to said target polynucleotide in the sample, and which probe specifically hybridizes to said target polynucleotide, under conditions whereby a hybridization complex is formed between said probe and said target polynucleotide or fragments thereof, and b) detecting the presence or absence of said hybridization complex, and optionally, if present, the amount thereof. In one alternative, the probe comprises at least 60 contiguous nucleotides.

[0044] The invention further provides a method for detecting a target polynucleotide in a sample, said target polynucleotide having a sequence of a polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:48-94, b) a naturally occurring polynucleotide comprising a polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:48-94, c) a polynucleotide complementary to the polynucleotide of a), d) a polynucleotide complementary to the polynucleotide of b), and e) an RNA equivalent of a)-d). The method comprises a) amplifying said target polynucleotide or fragment thereof using polymerase chain reaction amplification, and b) detecting the presence or absence of said amplified target polynucleotide or fragment thereof, and, optionally, if present, the amount thereof.

[0045] The invention further provides a composition comprising an effective amount of a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, b) a naturally occurring polypeptide comprising an amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, and a pharmaceutically acceptable excipient In one embodiment, the composition comprises an amino acid sequence selected from the group consisting of SEQ ID NO:1-47. The invention additionally provides a method of treating a disease or condition associated with decreased expression of functional RMEP, comprising administering to a patient in need of such treatment the composition.

[0046] The invention also provides a method for screening a compound for effectiveness as an agonist of a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, b) a naturally occurring polypeptide comprising an amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47. The method comprises a) exposing a sample comprising the polypeptide to a compound, and b) detecting agonist activity in the sample. In one alternative, the invention provides a composition comprising an agonist compound identified by the method and a pharmaceutically acceptable excipient In another alternative, the invention provides a method of treating a disease or condition associated with decreased expression of functional RMEP, comprising administering to a patient in need of such treatment the composition.

[0047] Additionally, the invention provides a method for screening a compound for effectiveness as an antagonist of a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, b) a naturally occurring polypeptide comprising an amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47. The method comprises a) exposing a sample comprising the polypeptide to a compound, and b) detecting antagonist activity in the sample. In one alternative, the invention provides a composition comprising an antagonist compound identified by the method and a pharmaceutically acceptable excipient In another alternative, the invention provides a method of treating a disease or condition associated with overexpression of functional RMEP, comprising administering to a patient in need of such treatment the composition.

[0048] The invention father provides a method of screening for a compound that specifically binds to a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, b) a naturally occurring polypeptide comprising an amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47. The method comprises a) combining the polypeptide with at least one test compound under suitable conditions, and b) detecting binding of the polypeptide to the test compound, thereby identifying a compound that specifically binds to the polypeptide.

[0049] The invention further provides a method of screening for a compound that modulates the activity of a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, b) a naturally occurring polypeptide comprising an amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47. The method comprises a) combining the polypeptide with at least one test compound under conditions permissive for the activity of the polypeptide, b) assessing the activity of the polypeptide in the presence of the test compound, and c) comparing the activity of the polypeptide in the presence of the test compound with the activity of the polypeptide in the absence of the test compound, wherein a change in the activity of the polypeptide in the presence of the test compound is indicative of a compound that modulates the activity of the polypeptide.

[0050] The invention further provides a method for screening a compound for effectiveness in altering expression of a target polynucleotide, wherein said target polynucleotide comprises a sequence selected from the group consisting of SEQ ID NO:48-94, the method comprising a) exposing a sample comprising the target polynucleotide to a compound, and b) detecting altered expression of the target polynucleotide.

[0051] The invention further provides a method for assessing toxicity of a test compound, said method comprising a) treating a biological sample containing nucleic acids with the test compound; b) hybridizing the nucleic acids of the treated biological sample with a probe comprising at least 20 contiguous nucleotides of a polynucleotide selected from the group consisting of i) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:48-94, ii) a naturally occurring polynucleotide comprising a polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:48-94, iii) a polynucleotide having a sequence complementary to i), iv) a polynucleotide complementary to the polynucleotide of ii), and v) an RNA equivalent of i)-iv). Hybridization occurs under conditions whereby a specific hybridization complex is formed between said probe and a target polynucleotide in the biological sample, said target polynucleotide selected from the group consisting of i) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:48-94, ii) a naturally occurring polynucleotide comprising a polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:48-94, iii) a polynucleotide complementary to the polynucleotide of i), iv) a polynucleotide complementary to the polynucleotide of ii), and v) an RNA equivalent of i)-iv). Alternatively, the target polynucleotide comprises a fragment of a polynucleotide sequence selected from the group consisting of i)-v) above; c) quantifying the amount of hybridization complex; and d) comparing the amount of hybridization complex in the treated biological sample with the amount of hybridization complex in an untreated biological sample, wherein a difference in the amount of hybridization complex in the treated biological sample is indicative of toxicity of the test compound.

BRIEF DESCRIPTION OF THE TABLES

[0052] Table 1 summarizes the nomenclature for the full length polynucleotide and polypeptide sequences of the present invention.

[0053] Table 2 shows the GenBank identification number and annotation of the nearest GenBank homolog for polypeptides of the invention. The probability score for the match between each polypeptide and its GenBank homolog is also shown.

[0054] Table 3 shows structural features of polypeptide sequences of the invention, including predicted motifs and domains, along with the methods, algorithms, and searchable databases used for analysis of the polypeptides.

[0055] Table 4 lists the cDNA fragments which were used to assemble polynucleotide sequences of the invention, along with selected fragments of the polynucleotide sequences.

[0056] Table 5 shows the representative cDNA library for polynucleotides of the invention.

[0057] Table 6 provides an appendix which describes the tissues and vectors used for construction of the cDNA libraries shown in Table 5.

[0058] Table 7 shows the tools, programs, and algorithms used to analyze the polynucleotides and polypeptides of the invention, along with applicable descriptions, references, and threshold parameters.

DESCRIPTION OF THE INVENTION

[0059] Before the present proteins, nucleotide sequences, and methods are described, it is understood that this invention is not limited to the particular machines, materials and methods described, as these may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention which will be, limited only by the appended claims.

[0060] It must be noted that as used herein and in the appended claims, the singular forms “a,” “an,” and “the” include plural reference unless the context clearly dictates otherwise. Thus, for example, a reference to “a host cell” includes a plurality of such host cells, and a reference to “an antibody” is a reference to one or more antibodies and equivalents thereof known to those skilled in the art, and so forth.

[0061] Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any machines, materials, and methods similar or equivalent to those described herein can be used to practice or test the present invention, the preferred machines, materials and methods are now described. All publications mentioned herein are cited for the purpose of describing and disclosing the cell lines, protocols, reagents and vectors which are reported in the publications and which might be used in connection with the invention. Nothing herein is to be construed as an admission that the invention is not entitled to antedate such disclosure by virtue of prior invention.

[0062] Definitions

[0063] “RMEP” refers to the amino acid sequences of substantially purified RMEP obtained from any species, particularly a mammalian species, including bovine, ovine, porcine, murine, equine, and human, and from any source, whether natural, synthetic, semi-synthetic, or recombinant.

[0064] The term “agonist” refers to a molecule which intensifies or mimics the biological activity of RMEP. Agonists may include proteins, nucleic acids, carbohydrates, small molecules, or any other compound or composition which modulates the activity of RMEP either by directly interacting with RMEP or by acting on components of the biological pathway in which RMEP participates.

[0065] An “allelic variant” is an alternative form of the gene encoding RMEP. Allelic variants may result from at least one mutation in the nucleic acid sequence and may result in altered mRNAs or in polypeptides whose structure or function may or may not be altered. A gene may have none, one, or many allelic variants of its naturally occurring form Common mutational changes which give rise to allelic variants are generally ascribed to natural deletions, additions, or substitutions of nucleotides. Each of these types of changes may occur alone, or in combination with the others, one or more times in a given sequence.

[0066] “Altered” nucleic acid sequences encoding RMEP include those sequences with deletions, insertions, or substitutions of different nucleotides, resulting in a polypeptide the same as RMEP or a polypeptide with at least one functional characteristic of RMEP. Included within this definition are polymorphisms which may or may not be readily detectable using a particular oligonucleotide probe of the polynucleotide encoding RMEP, and improper or unexpected hybridization to allelic variants, with a locus other than the normal chromosomal locus for the polynucleotide sequence encoding RMEP. The encoded protein may also be “altered,” and may contain deletions, insertions, or substitutions of amino acid residues which produce a silent change and result in a functionally equivalent RMEP. Deliberate amino acid substitutions may be made on the basis of similarity in polarity, charge, solubility, hydrophobicity, hydrophilicity, and/or the amphipathic nature of the residues, as long as the biological or immunological activity of RMEP is retained. For example, negatively charged amino acids may include aspartic acid and glutamic acid, and positively charged amino acids may include lysine and arginine. Amino acids with uncharged polar side chains having similar hydrophilicity values may include: asparagine and glutamine; and serine and tbreonine. Amino acids with uncharged side chains having similar hydrophilicity values may include: leucine, isoleucine, and valine; glycine and alanine; and phenylalanine and tyrosine.

[0067] The terms “amino acid” and “amino acid sequence” refer to an oligopeptide, peptide, polypeptide, or protein sequence, or a fragment of any of these, and to naturally occurring or synthetic molecules. Where “amino acid sequence” is recited to refer to a sequence of a naturally occurring protein molecule, “amino acid sequence” and like terms are not meant to limit the amino acid sequence to the complete native amino acid sequence associated with the recited protein molecule.

[0068] “Amplification” relates to the production of additional copies of a nucleic acid sequence. Amplification is generally carried out using polymerase chain reaction (PCR) technologies well known in the art.

[0069] The term “antagonist” refers to a molecule which inhibits or attenuates the biological activity of RMEP. Antagonists may include proteins such as antibodies, nucleic acids, carbohydrates, small molecules, or any other compound or composition which modulates the activity of RMEP either by directly interacting with RMEP or by acting on components of the biological pathway in which RMEP participates.

[0070] The term “antibody” refers to intact immunoglobulin molecules as well as to fragments thereof, such as Fab, F(ab′)₂, and Fv fragments, which are capable of binding an epitopic determinant. Antibodies that bind RMEP polypeptides can be prepared using intact polypeptides or using fragments containing small peptides of interest as the immunizing antigen. The polypeptide or oligopeptide used to immunize an animal (e.g., a mouse, a rat, or a rabbit) can be derived from the translation of RNA, or synthesized chemically, and can be conjugated to a carrier protein if desired. Commonly used carriers that are chemically coupled to peptides include bovine serum albumin, thyroglobulin, and keyhole limpet hemocyanin (KLH). The coupled peptide is then used to immunize the animal.

[0071] The term “antigenic determinant” refers to that region of a molecule (i.e., an epitope) that makes contact with a particular antibody. When a protein or a fragment of a protein is used to immunize a host animal, numerous regions of the protein may induce the production of antibodies which bind specifically to antigenic determinants (particular regions or three-dimensional structures on the protein). An antigenic determinant may compete with the intact antigen (i.e., the immunogen used to elicit the immune response) for binding to an antibody.

[0072] The term “antisense” refers to any composition capable of base-pairing with the “sense” (coding) strand of a specific nucleic acid sequence. Antisense compositions may include DNA; RNA; peptide nucleic acid (PNA); oligonucleotides having modified backbone linkages such as phosphorotbioates, methylphosphonates, or benzylphosphonates; oligonucleotides having modified sugar groups such as 2 ′-methoxyethyl sugars or 2 ′-methoxyethoxy sugars; or oligonucleotides having modified bases such as 5-methyl cytosine, 2′-deoxyuracil, or 7-deaza-2′-deoxyguanosine. Antisense molecules may be produced by any method including chemical synthesis or transcription. Once introduced into a cell, the complementary antisense molecule base-pairs with a naturally occurring nucleic acid sequence produced by the cell to form duplexes which block either transcription or translation The designation “negative” or “minus” can refer to the antisense strand, and the designation “positive” or “plus” can refer to the sense strand of a reference DNA molecule.

[0073] The term “biologically active” refers to a protein having structural, regulatory, or biochemical functions of a naturally occurring molecule. Likewise, “immunologically active” or “immunogenic” refers to the capability of the natural, recombinant, or synthetic RMEP, or of any oligopeptide thereof, to induce a specific immune response in appropriate animals or cells and to bind with specific antibodies.

[0074] “Complementary” describes the relationship between two single-stranded nucleic acid sequences that anneal by base-pairing. For example, 5′-AGT-3′ pairs with its complement, 3′-TCA-5′.

[0075] A “composition comprising a given polynucleotide sequence” and a “composition comprising a given amino acid sequence” refer broadly to any composition containing the given polynucleotide or amino acid sequence. The composition may comprise a dry formulation or an aqueous solution. Compositions comprising polynucleotide sequences encoding RMEP or fragments of RMEP may be employed as hybridization probes. The probes may be stored in freeze-dried form and may be associated with a stabilizing agent such as a carbohydrate. In hybridizations, the probe may be deployed in an aqueous solution containing salts (e.g., NaCl), detergents (e.g., sodium dodecyl sulfate; SDS), and other components (e.g., Denbardt's solution, dry milk, salmon sperm DNA, etc.).

[0076] “Consensus sequence” refers to a nucleic acid sequence which has been subjected to repeated DNA sequence analysis to resolve uncalled bases, extended using the XL-PCR kit (Applied Biosystems, Foster City Calif.) in the 5′ and/or the 3′ direction, and resequenced, or which has been assembled from one or more overlapping eDNA, EST, or genomic DNA fragments using a computer program for fragment assembly, such as the GELVIEW fragment assembly system (GCG, Madison Wis.) or Phrap (University of Washington, Seattle Wash.). Some sequences have been both extended and assembled to produce the consensus sequence.

[0077] “Conservative amino acid substitutions” are those substitutions that are predicted to least interfere with the properties of the original protein, i.e., the structure and especially the function of the protein is conserved and not significantly changed by such substitutions. The table below shows amino acids which may be substituted for an original amino acid in a protein and which are regarded as conservative amino acid substitutions. Original Residue Conservative Substitution Ala Gly, Ser Arg His, Lys Asn Asp, Gln, His Asp Asn, Glu Cys Ala, Ser Gln Asn, Glu, His Glu Asp, Gln, His Gly Ala His Asn, Arg, Gln, Glu Ile Leu, Val Leu Ile, Val Lys Arg, Gln, Glu Met Leu, Ile Phe His, Met, Leu, Trp, Tyr Ser Cys, Thr Thr Ser, Val Trp Phe, Tyr Tyr His, Phe, Trp Val Ile, Leu, Thr

[0078] Conservative amino acid substitutions generally maintain (a) the structure of the polypeptide backbone in the area of the substitution, for example, as a beta sheet or alpha helical conformation, (b) the charge or hydrophobicity of the molecule at the site of the substitution, and/or (c) the bulk of the side chain.

[0079] A “deletion” refers to a change in the amino acid or nucleotide sequence that results in the absence of one or more amino acid residues or nucleotides.

[0080] The term “derivative” refers to a chemically modified polynucleotide or polypeptide. Chemical modifications of a polynucleotide can include, for example, replacement of hydrogen by an alkyl, acyl, hydroxyl, or amino group. A derivative polynucleotide encodes a polypeptide which retains at least one biological or immunological function of the natural molecule. A derivative polypeptide is one modified by glycosylation, pegylation, or any similar process that retains at least one biological or immunological function of the polypeptide from which it was derived.

[0081] A “detectable label” refers to a reporter molecule or enzyme that is capable of generating a measurable signal and is covalently or noncovalently joined to a polynucleotide or polypeptide.

[0082] “Differential expression” refers to increased or upregulated; or decreased, downregulated, or absent gene or protein expression, determined by comparing at least two different samples. Such comparisons may be carried out between, for example, a treated and an untreated sample, or a diseased and a normal sample.

[0083] A “fragment” is a unique portion of RMEP or the polynucleotide encoding RMEP which is identical in sequence to but shorter in length than the parent sequence. A fragment may comprise up to the entire length of the defined sequence, minus one nucleotide/amino acid residue. For example, a fragment may comprise from 5 to 1000 contiguous nucleotides or amino acid residues. A fragment used as a probe, primer, antigen, therapeutic molecule, or for other purposes, may be at least 5, 10, 15, 16, 20, 25, 30, 40, 50, 60, 75, 100, 150, 250 or at least 500 contiguous nucleotides or amino acid residues in length. Fragments may be preferentially selected from certain regions of a molecule. For example, a polypeptide fragment may comprise a certain length of contiguous amino acids selected from the first 250 or 500 amino acids (or first 25% or 50%) of a polypeptide as shown in a certain defined sequence. Clearly these lengths are exemplary, and any length that is supported by the specification, including the Sequence Listing, tables, and figures, may be encompassed by the present embodiments.

[0084] A fragment of SEQ ID NO:48-94 comprises a region of unique polynucleotide sequence that specifically identifies SEQ ID NO:48-94, for example, as distinct from any other sequence in the genome from which the fragment was obtained. A fragment of SEQ ID NO:48-94 is useful, for example, in hybridization and amplification technologies and in analogous methods that distinguish SEQ ID NO:48-94 from related polynucleotide sequences. The precise length of a fragment of SEQ ID NO:48-94 and the region of SEQ ID NO:48-94 to which the fragment corresponds are routinely determinable by one of ordinary skill in the art based on the intended purpose for the fragment.

[0085] A fragment of SEQ ID NO:1-47 is encoded by a fragment of SEQ ID NO:48-94. A fragment of SEQ ID NO:1-47 comprises a region of unique amino acid sequence that specifically identifies SEQ ID NO:1-47. For example, a fragment of SEQ ID NO:1-47 is useful as an immunogenic peptide for the development of antibodies that specifically recognize SEQ ID NO:1-47. The precise length of a fragment of SEQ ID NO:1-47 and the region of SEQ ID NO:1-47 to which the fragment corresponds are routinely determinable by one of ordinary skill in the art based on the intended purpose for the fragment.

[0086] A “full length” polynucleotide sequence is one containing at least a translation initiation codon. (e.g., methionine) followed by an open reading frame and a translation termination codoil A “full length” polynucleotide sequence encodes a “full length” polypeptide sequence.

[0087] “Homology” refers to sequence similarity or, interchangeably, sequence identity, between two or more polynucleotide sequences or two or more polypeptide sequences.

[0088] The terms “percent identity” and “% identity,” as applied to polynucleotide sequences, refer to the percentage of residue matches between at least two polynucleotide sequences aligned using a standardized algorithm Such an algorithm may insert, in a standardized and reproducible way, gaps in the sequences being compared in order to optimize alignment between two sequences, and therefore achieve a more meaningful comparison of the two sequences.

[0089] Percent identity between polynucleotide sequences may be determined using the default parameters of the CLUSTAL V algorithm as incorporated into the MEGALIGN version 3.12e sequence alignment program. This program is part of the LASERGENE software package, a suite of molecular biological analysis programs (DNASTAR, Madison Wis.). CLUSTAL V is described in Higgins, D. G. and P. M. Sharp (1989) CABIOS 5:151-153 and in Higgins, D. G. et al. (1992) CABIOS 8:189-191. For pairwise alignments of polynucleotide sequences, the default parameters are set as follows: Ktuple=2, gap penalty=5, window=4, and “diagonals saved”=4. The “weighted” residue weight table is selected as the default. Percent identity is reported by CLUSTAL V as the “percent similarity” between aligned polynucleotide sequences.

[0090] Alternatively, a suite of commonly used and freely available sequence comparison algorithms is provided by the National Center for Biotechnology Information (NCBI) Basic Local Alignment Search Tool (BLAST) (Altschul, S. F. et al. (1990) J. Mol. Biol. 215:403-410), which is available from several sources, including the NCBI, Bethesda, Md., and on the Internet at http://www.ncbi.nlm.nih.gov/BLAST/. The BLAST software suite includes various sequence analysis programs including “blastn,” that is used to align a known polynucleotide sequence with other polynucleotide sequences from a variety of databases. Also available is a tool called “BLAST 2 Sequences” that is used for direct pairwise comparison of two nucleotide sequences. “BLAST 2 Sequences” can be accessed and used interactively at http://www.ncbi.nlm.nih.gov/gorf/b12. html. The “BLAST 2 Sequences” tool can be used for both blastn and blastp (discussed below). BLAST programs are commonly used with gap and other parameters set to default settings. For example, to compare two nucleotide sequences, one may use blasta with the “BLAST 2 Sequences” tool Version 2.0.12 (Apr. 21, 2000) set at default parameters. Such default parameters may be, for example:

[0091] Matrix: BLOSUM62

[0092] Reward for match: 1

[0093] Penalty for mismatch:−2

[0094] Open Gap: 5 and Extension Gap: 2 penalties

[0095] Gap x drop-off: 50

[0096] Expect: 10

[0097] Word Size: 11

[0098] Filter: on

[0099] Percent identity may be measured over the length of an entire defined sequence, for example, as defined by a particular SEQ ID number, or may be measured over a shorter length, for example, over the length of a fragment taken from a larger, defined sequence, for instance, a fragment of at least 20, at least 30, at least 40, at least 50, at least 70, at least 100, or at least 200 contiguous nucleotides. Such lengths are exemplary only, and it is understood that any fragment length supported by the sequences shown herein, in the tables, figures, or Sequence Listing, may be used to describe a length over which percentage identity may be measured.

[0100] Nucleic acid sequences that do not show a high degree of identity may nevertheless encode similar amino acid sequences due to the degeneracy of the genetic code. It is understood that changes in a nucleic acid sequence can be made using this degeneracy to produce multiple nucleic acid sequences that all encode substantially the same protein.

[0101] The phrases “percent identity” and “% identity,” as applied to polypeptide sequences, refer to the percentage of residue matches between at least two polypeptide sequences aligned using a standardized algorithm Methods of polypeptide sequence alignment are well-known. Some alignment methods take into account conservative amino acid substitutions. Such conservative substitutions, explained in more detail above, generally preserve the charge and hydrophobicity at the site of substitution, thus preserving the structure (and therefore function) of the polypeptide.

[0102] Percent identity between polypeptide sequences may be determined using the default parameters of the CLUSTAL V algorithm as incorporated into the MEGALIGN version 3.12e sequence alignment program (described and referenced above). For pairwise alignments of polypeptide sequences using CLUSTAL V, the default parameters are set as follows: Ktuple=1, gap penalty=3, window=5, and “diagonals saved”=5. The PAM250 matrix is selected as the default residue weight table. As with polynucleotide alignments, the percent identity is reported by CLUSTAL V as the “percent similarity” between aligned polypeptide sequence pairs.

[0103] Alternatively the NCBI BLAST software suite may be used, For example, for a pairwise comparison of two polypeptide sequences, one may use the “BLAST 2 Sequences” tool Version 2.0.12 (Apr. 21, 2000) with blastp set at default parameters. Such default parameters may be, for example:

[0104] Matrix: BLOSUM62

[0105] Open Gap: 11 and Extension Gap: 1 penalties

[0106] Gap x drop-off: 50

[0107] Expect: 10

[0108] Word Size: 3

[0109] Filter: on

[0110] Percent identity may be measured over the length of an entire defined polypeptide sequence, for example, as defined by a particular SEQ ID number, or may be measured over a shorter length, for example, over the length of a fragment taken from a larger, defined polypeptide sequence, for instance, a fragment of at least 15, at least 20, at least 30, at least 40, at least 50, at least 70 or at least 150 contiguous residues. Such lengths are exemplary only, and it is understood that any fragment length supported by the sequences shown herein, in the tables, figures or Sequence Listing, may be used to describe a length over which percentage identity may be measured.

[0111] “Human artificial chromosomes” (HACs) are linear microchromosomes which may contain DNA sequences of about 6 kb to 10 Mb in size and which contain all of the elements required for chromosome replication, segregation and maintenance.

[0112] The term “humanized antibody” refers to an antibody molecule in which the amino acid sequence in the non-antigen binding regions has been altered so that the antibody more closely resembles a human antibody, and still retains its original binding ability.

[0113] “Hybridization” refers to the process by which a polynucleotide strand anneals with a complementary strand through base pairing under defined hybridization conditions. Specific hybridization is an indication that two nucleic acid sequences share a high degree of complementarity. Specific hybridization complexes form under permissive annealing conditions and remain hybridized after the “washing” step(s). The washing step(s) is particularly important in determining the stringency of the hybridization process, with more stringent conditions allowing less non-specific binding, i.e., binding between pairs of nucleic acid strands that are not perfectly matched. Permissive conditions for annealing of nucleic acid sequences are routinely determinable by one of ordinary skill in the art and may be consistent among hybridization experiments, whereas wash conditions may be varied among experiments to achieve the desired stringency, and therefore hybridization specificity. Permissive annealing conditions occur, for example, at 68° C. in the presence of about 6×SSC, about 1% (w/v) SDS, and about 100 μg/ml sheared, denatured salmon sperm DNA.

[0114] Generally, stringency of hybridization is expressed, in part, with reference to the temperature under which the wash step is carried out. Such wash temperatures are typically selected to be about 5° C. to 20° C. lower than the thermal melting point (T_(m)) for the specific sequence at a defined ionic strength and pH. The T_(m) is the temperature (under defined ionic strength and pH) at which 50% of the target sequence hybridizes to a perfectly matched probe. An equation for calculating T_(m) and conditions for nucleic acid hybridization are well known and can be found in Sambrook J. et al. (1989) Molecular Cloning: A Laboratory Manual, 2^(nd) ed., vol. 1-3, Cold Spring Harbor Press, Plainview N.Y.; specifically see volume 2, chapter 9.

[0115] High stringency conditions for hybridization between polynucleotides of the present invention include wash conditions of 68° C. in the presence of about 0.2×SSC and about 0.1% SDS, for 1 hour. Alternatively, temperatures of about 65° C., 60° C., 55° C., or 42° C. may be used SSC concentration may be varied from about 0.1 to 2×SSC, with SDS being present at about 0.1%. Typically, blocking reagents are used to block non-specific hybridization. Such blocking reagents include, for instance, sheared and denatured salmon sperm DNA at about 100-200 μg/ml. Organic solvent, such as formamide at a concentration of about 35-50% v/v, may also be used under particular circumstances, such as for RNA:DNA hybridizations. Useful variations on these wash conditions will be readily apparent to those of ordinary skill in the art. Hybridization, particularly under high stringency conditions, may be suggestive of evolutionary similarity between the nucleotides. Such similarity is strongly indicative of a similar role for the nucleotides and their encoded polypeptides.

[0116] The term “hybridization complex” refers to a complex formed between two nucleic acid sequences by virtue of the formation of hydrogen bonds between complementary bases. A hybridization complex may be formed in solution (e.g., C_(o) t or R_(o) t analysis) or formed between one nucleic acid sequence present in solution and another nucleic acid sequence immobilized on a solid support (e.g., paper, membranes, filters, chips, pins or glass slides, or any other appropriate substrate to which cells or their nucleic acids have been fixed).

[0117] The words “insertion” and “addition” refer to changes in an amino acid or nucleotide sequence resulting in the addition of one or more amino acid residues or nucleotides, respectively.

[0118] “Immune response” can refer to conditions associated with inflammation, trauma, immune disorders, or infectious or genetic disease, etc. These conditions can be characterized by expression of various factors, e.g., cytokines, chemokines, and other signaling molecules, which may affect cellular and systemic defense systems.

[0119] An “immunogenic fragment” is a polypeptide or oligopeptide fragment of RMEP which is capable of eliciting an immune response when introduced into a living organism, for example, a mammal. The term “immunogenic fragment” also includes any polypeptide or oligopeptide fragment of RMEF which is useful in any of the antibody production methods disclosed herein or known in the art.

[0120] The term “microarray” refers to an arrangement of a plurality of polynucleotides, polypeptides, or other chemical compounds on a substrate.

[0121] The terms “element” and “array element” refer to a polynucleotide, polypeptide, or other chemical compound having a unique and defined position on a microarray.

[0122] The term “modulate” refers to a change in the activity of RMEP. For example, modulation may cause an increase or a decrease in protein activity, binding characteristics, or any other biological, functional, or immunological properties of RMEP.

[0123] The phrases “nucleic acid” and “nucleic acid sequence” refer to a nucleotide, oligonucleotide, polynucleotide, or any fragment thereof. These phrases also refer to DNA or RNA of genomic or synthetic origin which may be single-stranded or double-stranded and may represent the sense or the antisense strand, to peptide nucleic acid (PNA), or to any DNA-like or RNA-like material.

[0124] “Operably linked” refers to the situation in which a first nucleic acid sequence is placed in a functional relationship with a second nucleic acid sequence. For instance, a promoter is operably linked to a coding sequence if the promoter affects the transcription or expression of the coding sequence. Operably linked DNA sequences may be in close proximity or contiguous and, where necessary to join two protein coding regions, in the same reading frame.

[0125] “Peptide nucleic acid” (PNA) refers to an antisense molecule or anti-gene agent which comprises an oligonucleotide of at least about 5 nucleotides in length linked to a peptide backbone of amino acid residues ending in lysine. The terminal lysine confers solubility to the composition. PNAs preferentially bind complementary single stranded DNA or RNA and stop transcript elongation, and may be pegylated to extend their lifespan in the cell.

[0126] “Post-translational modification” of an RMEP may involve lipidation, glycosylation, phosphorylation, acetylation, radicalization, proteolytic cleavage, and other modifications known in the art. These processes may occur synthetically or biochemically. Biochemical modifications will vary by cell type depending on the enzymatic milieu of RMEP.

[0127] “Probe” refers to nucleic acid sequences encoding RMEP, their complements, or fragments thereof, which are used to detect identical, allelic or related nucleic acid sequences. Probes are isolated oligonucleotides or polynucleotides attached to a detectable label or reporter molecule. Typical labels include radioactive isotopes, ligands, chemiluminescent agents, and enzymes. “Primers” are short nucleic acids, usually DNA oligonucleotides, which may be annealed to a target polynucleotide by complementary base-pairing. The primer may then be extended along the target DNA strand by a DNA polymerase enzyme. Primer pairs can be used for amplification (and identification) of a nucleic acid sequence, e.g., by the polymerase chain reaction (PCR).

[0128] Probes and primers as used in the present invention typically comprise at least 15 contiguous nucleotides of a known sequence. In order to enhance specificity, longer probes and primers may also be employed, such as probes and primers that comprise at least 20, 25, 30, 40, 50, 60, 70, 80, 90, 100, or at least 150 consecutive nucleotides of the disclosed nucleic acid sequences. Probes and primers may be considerably longer than these examples, and it is understood that any length supported by the specification, including the tables, figures, and Sequence Listing, may be used.

[0129] Methods for preparing and using probes and primers are described in the references, for example Sambrook, J. et al. (1989) Molecular Cloning: A Laboratory Manual, 2^(nd) ed., vol. 1-3, Cold Spring Harbor Press, Plainview N.Y.; Ausubel, F. M. et al. (1987) Current Protocols in Molecular Biology, Greene Publ. Assoc. & Wiley-Intersciences, New York N.Y.; Innis, M. et al. (1990) PCR Protocols, A Guide to Methods and Applications, Academic Press, San Diego Calif. PCR primer pairs can be derived from a known sequence, for example, by using computer programs intended for that purpose such as Primer (Version 0.5, 1991, Whitehead Institute for Biomedical Research, Cambridge Mass.).

[0130] Oligonucleotides for use as primers are selected using software known in the art for such purpose. For example, OLIGO 4.06 software is useful for the selection of PCR primer pairs of up to 100 nucleotides each, and for the analysis of oligonucleotides and larger polynucleotides of up to 5,000 nucleotides from an input polynucleotide sequence of up to 32 kilobases. Similar primer selection programs have incorporated additional features for expanded capabilities. For example, the PrimOU primer selection program (available to the public from the Genome Center at University of Texas South West Medical Center, Dallas Tex.) is capable of choosing specific primers from megabase sequences and is thus useful for designing primers on a genome-wide scope. The Primer3 primer selection program (available to the public from the Whitehead Institute/MIT Center for Genome Research, Cambridge Mass.) allows the user to input a “mispriming library,” in which sequences to avoid as primer binding sites are user-specified. Primer3 is useful, in particular, for the selection of oligonucleotides for microarrays. (The source code for the latter two primer selection programs may also be obtained from their respective sources and modified to meet the user's specific needs.) The PrimeGen program (available to the public from the UK Human Genome Mapping Project Resource Centre, Cambridge UK) designs primers based on multiple sequence alignments, thereby allowing selection of primers that hybridize to either the most conserved or least conserved regions of aligned nucleic acid sequences. Hence, this program is useful for identification of both unique and conserved oligonucleotides and polynucleotide fragments. The oligonucleotides and polynucleotide fragments identified by any of the above selection methods are useful in hybridization technologies, for example, as PCR or sequencing primers, microarray elements, or specific probes to identify fully or partially complementary polynucleotides in a sample of nucleic acids. Methods of oligonucleotide selection are not limited to those described above.

[0131] A “recombinant nucleic acid” is a sequence that is not naturally occurring or has a sequence that is made by an artificial combination of two or more otherwise separated segments of sequence. This artificial combination is often accomplished by chemical synthesis or, more commonly, by the artificial manipulation of isolated segments of nucleic acids, e.g., by genetic engineering techniques such as those described in Sambrook, supra. The term recombinant includes nucleic acids that have been altered solely by addition, substitution, or deletion of a portion of the nucleic acid. Frequently, a recombinant nucleic acid may include a nucleic acid sequence operably linked to a promoter sequence. Such a recombinant nucleic acid may be part of a vector that is used, for example, to transform a cell.

[0132] Alternatively, such recombinant nucleic acids may be part of a viral vector, e.g., based on a vaccinia virus, that could be use to vaccinate a mammal wherein the recombinant nucleic acid is expressed, inducing a protective immunological response in the mammal.

[0133] A “regulatory element” refers to a nucleic acid sequence usually derived from untranslated regions of a gene and includes enhancers, promoters, introns, and 5′ and 3′ untranslated regions (UTRs). Regulatory elements interact with host or viral proteins which control transcription, translation, or RNA stability.

[0134] “Reporter molecules” are chemical or biochemical moieties used for labeling a nucleic acid, amino acid, or antibody. Reporter molecules include radionuclides; enzymes; fluorescent, chemiluminescent, or chromogenic agents; substrates; cofactors; inhibitors; magnetic particles; and other moieties known in the art.

[0135] An “RNA equivalent,” in reference to a DNA sequence, is composed of the same linear sequence of nucleotides as the reference DNA sequence with the exception that all occurrences of the nitrogenous base thymine are replaced with uracil, and the sugar backbone is composed of ribose instead of deoxyribose.

[0136] The term “sample” is used in its broadest sense. A sample suspected of containing RMEP, nucleic acids encoding RMEP, or fragments thereof may comprise a bodily fluid; an extract from a cell, chromosome, organelle, or membrane isolated from a cell; a cell; genomic DNA, RNA, or cDNA, in solution or bound to a substrate; a tissue; a tissue print; etc.

[0137] The terms “specific binding” and “specifically binding” refer to that interaction between a protein or peptide and an agonist, an antibody, an antagonist, a small molecule, or any natural or synthetic binding composition. The interaction is dependent upon the presence of a particular structure of the protein, e.g., the antigenic determinant or epitope, recognized by the binding molecule. For example, if an antibody is specific for epitope “A,” the presence of a polypeptide comprising the epitope A, or the presence of free unlabeled A, in a reaction containing free labeled A and the antibody will reduce the amount of labeled A that binds to the antibody.

[0138] The term “substantially purified” refers to nucleic acid or amino acid sequences that are removed from their natural environment and are isolated or separated, and are at least 60% free, preferably at least 75% free, and most preferably at least 90% free from other components with which they are naturally associated

[0139] A “substitution” refers to the replacement of one or more amino acid residues or nucleotides by different amino acid residues or nucleotides, respectively.

[0140] “Substrate” refers to any suitable rigid or semi-rigid support including membranes, filters, chips, slides, wafers, fibers, magnetic or nonmagnetic beads, gels, tubing, plates, polymers, microparticles and capillaries. The substrate can have a variety of surface forms, such as wells, trenches, pins, channels and pores, to which polynucleotides or polypeptides are bound.

[0141] A “transcript image” refers to the collective pattern of gene expression by a particular cell type or tissue under given conditions at a given time.

[0142] “Transformation” describes a process by which exogenous DNA is introduced into a recipient cell. Transformation may occur under natural or artificial conditions according to various methods well known in the art, and may rely on any known method for the insertion of foreign nucleic acid sequences into a prokaryotic or eukaryotic host cell. The method for transformation is selected based on the type of host cell being transformed and may include, but is not limited to, bacteriophage or viral infection, electroporation, heat shock, lipofection, and particle bombardment. The term “transformed cells” includes stably transformed cells in which the inserted DNA is capable of replication either as an autonomously replicating plasmid or as part of the host chromosome, as well as transiently transformed cells which express the inserted DNA or RNA for limited periods of time.

[0143] A “transgenic organism,” as used herein, is any organism, including but not limited to animals and plants, in which one or more of the cells of the organism contains heterologous nucleic acid introduced by way of human intervention, such as by transgenic techniques well known in the art. The nucleic acid is introduced into the cell, directly or indirectly by introduction into a precursor of the cell, by way of deliberate genetic manipulation, such as by microinjection or by infection with a recombinant virus. The term genetic manipulation does not include classical cross-breeding, or in vitro fertilization, but rather is directed to the introduction of a recombinant DNA molecule. The transgenic organisms contemplated in accordance with the present invention include bacteria, cyanobacteria, fungi, plants and animals. The isolated DNA of the present invention can be introduced into the host by methods known in the art, for example infection, transfection, transformation or transconjugation. Techniques for transferring the DNA of the present invention into such organisms are widely known and provided in references such as Sambrook et al. (1989), supra.

[0144] A “variant” of a particular nucleic acid sequence is defined as a nucleic acid sequence having at least 40% sequence identity to the particular nucleic acid sequence over a certain length of one of the nucleic acid sequences using blastn with the “BLAST 2 Sequences” tool Version 2.0.9 (May 7, 1999) set at default parameters. Such a pair of nucleic acids may show, for example, at least 50%, at least 60%, at least 70%, at least 80%, at least 85%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% or greater sequence identity over a certain defined length. A variant may be described as, for example, an “allelic” (as defined above), “splice,” “species,” or “polymorphic” variant. A splice variant may have significant identity to a reference molecule, but will generally have a greater or lesser number of polynucleotides due to alternative splicing of exons during mRNA processing. The corresponding polypeptide may possess additional functional domains or lack domains that are present in the reference molecule. Species variants are polynucleotide sequences that vary from one species to another. The resulting polypeptides will generally have significant amino acid identity relative to each other. A polymorphic variant is a variation in the polynucleotide sequence of a particular gene between individuals of a given species. Polymorphic variants also may encompass “singe nucleotide polymorphisms” (SNPs) in which the polynucleotide sequence varies by one nucleotide base. The presence of SNPs may be indicative of, for example, a certain population, a disease state, or a propensity for a disease state.

[0145] A “variant” of a particular polypeptide sequence is defined as a polypeptide sequence having at least 40% sequence identity to the particular polypeptide sequence over a certain length of one of the polypeptide sequences using blastp with the “BLAST 2 Sequences” tool Version 2.0.9 (May 7, 1999) set at default parameters. Such a pair of polypeptides may show, for example, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% or greater sequence identity over a certain defined length of one of the polypeptides.

[0146] The Invention

[0147] The invention is based on the discovery of new human RNA metabolism proteins (RMEP), the polynucleotides encoding RMEP, and the use of these compositions for the diagnosis, treatment, or prevention of nervous system, autoimmune/inflammatory, cell proliferative, and developmental disorders.

[0148] Table 1 summarizes the nomenclature for the full length polynucleotide and polypeptide sequences of the invention. Each polynucleotide and its corresponding polypeptide are correlated to a single Incyte project identification number (Incyte Project ID). Each polypeptide sequence is denoted by both a polypeptide sequence identification number (Polypeptide SEQ ID NO:) and an Incyte polypeptide sequence number (Incyte Polypeptide ID) as shown. Each polynucleotide sequence is denoted by both a polynucleotide sequence identification number (Polynucleotide SEQ ID NO:) and an Incyte polynucleotide consensus sequence number (Incyte Polynucleotide ID) as shown.

[0149] Table 2 shows sequences with homology to the polypeptides of the invention as identified by BLAST analysis against the GenBank protein (genpept) database. Columns 1 and 2 show the polypeptide sequence identification number (Polypeptide SEQ ID NO:) and the corresponding Incyte polypeptide sequence number (Incyte Polypeptide ID) for polypeptides of the invention Column 3 shows the GenBank identification number (Genbank ID NO:) of the nearest GenBank homolog. Column 4 shows the probability score for the match between each polypeptide and its GenBank homolog. Column 5 shows the annotation of the GenBank homolog along with relevant citations where applicable, all of which are expressly incorporated by reference herein.

[0150] Table 3 shows various structural features of the polypeptides of the invention. Columns 1 and 2 show the polypeptide sequence identification number (SEQ ID NO:) and the corresponding Incyte polypeptide sequence number (Incyte Polypeptide ID) for each polypeptide of the invention. Column 3 shows the number of amino acid residues in each polypeptide. Column 4 shows potential phosphorylation sites, and column 5 shows potential glycosylation sites, as determined by the MOTIFS program of the GCG sequence analysis software package (Genetics Computer Group, Madison Wis.). Column 6 shows amino acid residues comprising signature sequences, domains, and motifs. Column 7 shows analytical methods for protein structural/function analysis and in some cases, searchable databases to which the analytical methods were applied.

[0151] Together, Tables 2 and 3 summarize the properties of polypeptides of the invention, and these properties establish that the claimed polypeptides are RNA metabolism proteins. SEQ ID NO:46 is 29% identical to Glu-tRNA^(Gln) amidotransferase, subunit A, of Neisseria meningitidis (GenBank ID g7226601) as determined by the Basic Local Alignment Search Tool (BLAST, see Table 2). The BLAST probability score is 1.3e-37, which indicates the probability of obtaining the observed polypeptide sequence alignment by chance. SEQ ID NO:46 also contains amidase signature sequences as determined by searching for statistically significant matches in the hidden Markov model (HMM)-based PFAM database of conserved protein family domains (see Table 3). Data from BLIMPS and PROFILESCAN analyses provide further corroborative evidence that SEQ ID NO:46 contains amidase signature sequences, features of polypeptides involved in transamidation reactions. These data provide evidence that SEQ ID NO:46 is related to the Glu-tRNA^(Gln) amidotransferases found in prokaryotes and some cellular organelles but, until the instant invention, not in humans. SEQ ID NO:47 is 97% identical to the 60S acidic ribosomal protein of Zea mays (GenBank ID g790508) as determined by the Basic Local Alignment Search Tool (BLAST, see Table 2). The BLAST probability score is 5.4e-51. SEQ ID NO:47 also contains a 60S acidic ribosomal protein domain as determined by searching for statistically significant matches in the hidden Markov model (HMM)-based PFAM database of conserved protein family domains (see Table 3). Data from BLIMPS analyses provide further corroborative evidence that SEQ ID NO:47 is a phosphorylated (hence likely to be acidic) ribosomal protein. SEQ ID NO:1-45 were analyzed and annotated in a similar manner. The algorithms and parameters for the analysis of SEQ ID NO:1-47 are described in Table 7.

[0152] As shown in Table 4, the full length polynucleotide sequences of the present invention were assembled using cDNA sequences or coding (exon) sequences derived from genomic DNA, or any combination of these two types of sequences. Columns 1 and 2 list the polynucleotide sequence identification number (Polynucleotide SEQ ID NO:) and the corresponding Incyte polynucleotide consensus sequence number (Incyte Polynucleotide ID) for each polynucleotide of the invention Column 3 shows the length of each polynucleotide sequence in basepairs. Column 4 lists fragments of the polynucleotide sequences which are useful, for example, in hybridization or amplification technologies that identify SEQ ID NO:48-94 or that distinguish between SEQ ID NO:48-94 and related polynucleotide sequences. Column 5 shows identification numbers corresponding to cDNA sequences, coding sequences (exons) predicted from genomic DNA, and/or sequence assemblages comprised of both cDNA and genomic DNA. These sequences were used to assemble the full length polynucleotide sequences of the invention Columns 6 and 7 of Table 4 show the nucleotide start (5′) and stop (3′) positions of the cDNA sequences in column 5 relative to their respective full length sequences.

[0153] The identification numbers in Column 5 of Table 4 may refer specifically, for example, to Incyte cDNAs along with their corresponding cDNA libraries. For example, 642017H1 is the identification number of an Incyte cDNA sequence, and BRSTNOT03 is the cDNA library from which it is derived. Incyte cDNAs for which cDNA libraries are not indicated were derived from pooled cDNA libraries (e.g., 70822015V1). Alternatively, the identification numbers in column 5 may refer to GenBank cDNAs or ESTs (e.g., gl 136841) which contributed to the assembly of the full length polynucleotide sequences. Alternatively, the identification numbers in column 5 may refer to coding regions predicted by Genscan analysis of genomic DNA. The Genscan-predicted coding sequences may have been edited prior to assembly. (See Example IV.) Alternatively, the identification numbers in column 5 may refer to assemblages of both cDNA and Genscan-predicted exons brought together by an “exon stitching” algorithm (See Example V.) Alternatively, the identification numbers in column 5 may refer to assemblages of both cDNA and Genscan-predicted exons brought together by an “exon-stretching” algorithm (See Example V.) In some cases, Incyte cDNA coverage redundant with the sequence coverage shown in column 5 was obtained to confirm the final consensus polynucleotide sequence, but the relevant Incyte cDNA identification numbers are not shown.

[0154] Table 5 shows the representative cDNA libraries for those full length polynucleotide sequences which were assembled using Incyte cDNA sequences. The representative cDNA library is the Incyte cDNA library which is most frequently represented by the Incyte cDNA sequences which were used to assemble and confirm the above polynucleotide sequences. The tissues and vectors which were used to construct the eDNA libraries shown in Table 5 are described in Table 6.

[0155] The invention also encompasses RMEP variants. A preferred RMEP variant is one which has at least about 80%, or alternatively at least about 90%, or even at least about 95% amino acid sequence identity to the RMEP amino acid sequence, and which contains at least one functional or structural characteristic of RMEP.

[0156] The invention also encompasses polynucleotides which encode RMEP. In a particular embodiment, the invention encompasses a polynucleotide sequence comprising a sequence selected from the group consisting of SEQ ID NO:48-94, which encodes RMEP. The polynucleotide sequences of SEQ ID NO:48-94, as presented in the Sequence Listing, embrace the equivalent RNA sequences, wherein occurrences of the nitrogenous base thymine are replaced with uracil, and the sugar backbone is composed of ribose instead of deoxyribose.

[0157] The invention also encompasses a variant of a polynucleotide sequence encoding RMEP. In particular, such a variant polynucleotide sequence will have at least about 70%, or alternatively at least about 85%, or even at least about 95% polynucleotide sequence identity to the polynucleotide sequence encoding RMEP. A particular aspect of the invention encompasses a variant of a polynucleotide sequence comprising a sequence selected from the group consisting of SEQ ID NO:48-94 which has at least about 70%, or alternatively at least about 85%, or even at least about 95% polynucleotide sequence identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO:48-94. Any one of the polynucleotide variants described above can encode an amino acid sequence which contains at least one functional or structural characteristic of RMEP.

[0158] It will be appreciated by those skilled in the art that as a result of the degeneracy of the genetic code, a multitude of polynucleotide sequences encoding RMEP, some bearing minimal similarity to the polynucleotide sequences of any known and naturally occurring gene, may be produced. Thus, the invention contemplates each and every possible variation of polynucleotide sequence that could be made by selecting combinations based on possible codon choices. These combinations are made in accordance with the standard triplet genetic code as applied to the polynucleotide sequence of naturally occurring RMEP, and all such variations are to be considered as being specifically disclosed

[0159] Although nucleotide sequences which encode RMEP and its variants are generally capable of hybridizing to the nucleotide sequence of the naturally occurring RMEP under appropriately selected conditions of stringency, it may be advantageous to produce nucleotide sequences encoding RMEP or its derivatives possessing a substantially different codon usage, e.g., inclusion of non-naturally occurring codons. Codons may be selected to increase the rate at which expression of the peptide occurs in a particular prokaryotic or eukaryotic host in accordance with the frequency with which particular codons are utilized by the host. Other reasons for substantially altering the nucleotide sequence encoding RMEP and its derivatives without altering the encoded amino acid sequences include the production of RNA transcripts having more desirable properties, such as a greater half-life, than transcripts produced from the naturally occurring sequence.

[0160] The invention also encompasses production of DNA sequences which encode RMEP and RMEP derivatives, or fragments thereof, entirely by synthetic chemistry. After production, the synthetic sequence may be inserted into any of the many available expression vectors and cell systems using reagents well known in the art. Moreover, synthetic chemistry may be used to introduce mutations into a sequence encoding RMEP or any fragment thereof.

[0161] Also encompassed by the invention are polynucleotide sequences that are capable of hybridizing to the claimed polynucleotide sequences, and, in particular, to those shown in SEQ ID NO:48-94 and fragments thereof under various conditions of stringency. (See, e.g., Wahl, G. M. and S. L. Berger (1987) Methods Enzymol. 152:399-407; Kimmel, A. R. (1987) Methods Enzymol. 152:507-511.) Hybridization conditions, including annealing and wash conditions, are described in “Definitions.”

[0162] Methods for DNA sequencing are well known in the art and may be used to practice any of the embodiments of the invention. The methods may employ such enzymes as the Klenow fragment of DNA polymerase I, SEQUENASE (US Biochemical, Cleveland Ohio), Taq polymerase (Applied Biosystems), thermos table T7 polymerase (Amersham Pharmacia Biotech, Piscataway N.J.), or combinations of polymerases and proofreading exonucleases such as those found in the ELONGASE amplification system (Life Technologies, Gaithersburg Md.). Preferably, sequence preparation is automated with machines such as the MICROLAB 2200 liquid transfer system (Hamilton, Reno Nev.), PTC200 thermal cycler (MJ Research, Watertown Mass.) and ABI CATALYST 800 thermal cycler (Applied Biosystems). Sequencing is then carried out using either the ABI 373 or 377 DNA sequencing system (Applied Biosystems), the MEGABASE 1000 DNA sequencing system (Molecular Dynamics, Sunnyvale Calif.), or other systems known in the art The resulting sequences are analyzed using a variety of algorithms which are well known in the art. (See, e.g., Ausubel, F. M. (1997) Short Protocols in Molecular Biology, John Wiley & Sons, New York N.Y., unit 7.7; Meyers, R. A. (1995) Molecular Biology and Biotechnology, Wiley VCH, New York N.Y., pp. 856-853.)

[0163] The nucleic acid sequences encoding RMEP may be extended utilizing a partial nucleotide sequence and employing various PCR-based methods known in the art to detect upstream sequences, such as promoters and regulatory elements. For example, one method which may be employed, restriction-site PCR, uses universal and nested primers to amplify unknown sequence from genomic DNA within a cloning vector. (See, e.g., Sarkar, G. (1993) PCR Methods Applic. 2:318-322.) Another method, inverse PCR, uses primers that extend in divergent directions to amplify unknown sequence from a circularized template. The template is derived from restriction fragments comprising a known genomic locus and surrounding sequences. (See, e.g., Triglia, T. et al. (1988) Nucleic Acids Res. 16:8186.) A third method, capture PCR, involves PCR amplification of DNA fragments adjacent to known sequences inhuman and yeast artificial chromosome DNA. (See, e.g., Lagerstrom, M. et al. (1991) PCR Methods Applic. 1:111-119.) In this method, multiple restriction enzyme digestions and ligations may be used to insert an engineered double-stranded sequence into a region of unknown sequence before performing PCR. Other methods which may be used to retrieve unknown sequences are known in the art. (See, e.g., Parker, J. D. et al. (1991) Nucleic Acids Res. 19:3055-3060). Additionally, one may use PCR, nested primers, and PROMOTERFINDER libraries (Clontech, Palo Alto Calif.) to walk genomic DNA. This procedure avoids the need to screen libraries and is useful in finding intron/exon junctions. For all PCR-based methods, primers may be designed using commercially available software, such as OLIGO 4.06 primer analysis software (National Biosciences, Plymouth Minn.) or another appropriate program, to be about 22 to 30 nucleotides in length, to have a GC content of about 50% or more, and to anneal to the template at temperatures of about 68° C. to 72° C.

[0164] When screening for full length cDNAs, it is preferable to use libraries that have been size-selected to include larger cDNAs. In addition, random-primed libraries, which often include sequences containing the 5′ regions of genes, are preferable for situations in which an oligo d(T) library does not yield a full-length cDNA. Genomic libraries may be useful for extension of sequence into 5′ non-transcribed regulatory regions.

[0165] Capillary electrophoresis systems which are commercially available may be used to analyze the size or confirm the nucleotide sequence of sequencing or PCR products. In particular, capillary sequencing may employ flowable polymers for electrophoretic separation, four different nucleotide-specific, laser-stimulated fluorescent dyes, and a charge coupled device camera for detection of the emitted wavelengths. Output/light intensity may be converted to electrical signal using appropriate software (e.g., GENOTYPER and SEQUENCE NAVIGATOR, Applied Biosystems), and the entire process from loading of samples to computer analysis and electronic data display may be computer controlled. Capillary electrophoresis is especially preferable for sequencing small DNA fragments which may be present in limited amounts in a particular sample.

[0166] In another embodiment of the invention, polynucleotide sequences or fragments thereof which encode RMEP may be cloned in recombinant DNA molecules that direct expression of RMEP, or fragments or functional equivalents thereof, in appropriate host cells. Due to the inherent degeneracy of the genetic code, other DNA sequences which encode substantially the same or a functionally equivalent amino acid sequence may be produced and used to express RMEP.

[0167] The nucleotide sequences of the present invention can be engineered using methods generally known in the art in order to alter RMEP-encoding sequences for a variety of purposes including, but not limited to, modification of the cloning, processing, and/or expression of the gene product. DNA shuffling by random fragmentation and PCR reassembly of gene fragments and synthetic oligonucleotides may be used to engineer the nucleotide sequences. For example, oligonucleotide-mediated site-directed mutagenesis may be used to introduce mutations that create new restriction sites, alter glycosylation patterns, change codon preference, produce splice variants, and so forth.

[0168] The nucleotides of the present invention may be subjected to DNA shuffling techniques such as MOLECULARBREEDING (Maxygen Inc., Santa Clara Calif.; described in U.S. Pat. No. 5,837,458; Chang, C.-C. et al. (1999) Nat. Biotechnol. 17:793-797; Christians, F. C. et al. (1999) Nat. Biotechnol. 17:259-264; and Crameri, A. et al. (1996) Nat. Biotechnol. 14:315-319) to alter or improve the biological properties of RMEP, such as its biological or enzymatic activity or its ability to bind to other molecules or compounds. DNA shuffling is a process by which a library of gene variants is produced using PCR-mediated recombination of gene fragments. The library is then subjected to selection or screening procedures that identify those gene variants with the desired properties. These preferred variants may then be pooled and further subjected to recursive rounds of DNA shuffling and selection/screening. Thus, genetic diversity is created through “artificial” breeding and rapid molecular evolution. For example, fragments of a single gene containing random point mutations may be recombined, screened, and then reshuffled until the desired properties are optimized. Alternatively, fragments of a given gene may be recombined with fragments of homologous genes in the same gene family, either from the same or different species, thereby maximizing the genetic diversity of multiple naturally occurring genes in a directed and controllable manner.

[0169] In another embodiment, sequences encoding RMEP may be synthesized, in whole or in part, using chemical methods well known in the art. (See, e.g., Caruthers, M. H. et al. (1980) Nucleic Acids Symp. Ser. 7:215-223; and Horn, T. et al. (1980) Nucleic Acids Symp. Ser. 7:225-232.) Alternatively, RMEP itself or a fragment thereof may be synthesized using chemical methods. For example, peptide synthesis can be performed using various solution-phase or solid-phase techniques. (See, e.g., Creighton, T. (1984) Proteins, Structures and Molecular Properties, W. H. Freeman, New York N.Y., pp. 55-60; and Roberge, J. Y. et al. (1995) Science 269:202-204.) Automated synthesis may be achieved using the ABI 431 A peptide synthesizer (Applied Biosystems). Additionally, the amino acid sequence of RMEP, or any part thereof, may be altered during direct synthesis and/or combined with sequences from other proteins, or any part thereof, to produce a variant polypeptide or a polypeptide having a sequence of a naturally occurring polypeptide.

[0170] The peptide may be substantially purified by preparative high performance liquid chromatography. (See, e.g., Chiez, R. M. and F. Z. Regnier (1990) Methods Enzymol. 182:392-421.) The composition of the synthetic peptides may be confirmed by amino acid analysis or by sequencing. (See, e.g., Creighton, supra, pp. 28-53.)

[0171] In order to express a biologically active RMEP, the nucleotide sequences encoding RMEP or derivatives thereof may be inserted into an appropriate expression vector, i.e., a vector which contains the necessary elements for transcriptional and translational control of the inserted coding sequence in a suitable host These elements include regulatory sequences, such as enhancers, constitutive and inducible promoters, and 5′ and 3′ untranslated regions in the vector and in polynucleotide sequences encoding RMEP. Such elements may vary in their strength and specificity. Specific initiation signals may also be used to achieve more efficient translation of sequences encoding RMEP. Such signals include the ATG initiation codon and adjacent sequences, e.g. the Kozak sequence. In cases where sequences encoding RMEP and its initiation codon and upstream regulatory sequences are inserted into the appropriate expression vector, no additional transcriptional or translational control signals may be needed. However, in cases where only coding sequence, or a fragment thereof, is inserted, exogenous translational control signals including an in-frame ATG initiation codon should be provided by the vector. Exogenous translational elements and initiation codons may be of various origins, both natural and synthetic. The efficiency of expression may be enhanced by the inclusion of enhancers appropriate for the particular host cell system used. (See, e.g., Scharf, D. et al. (1994) Results Probl. Cell Differ. 20:125-162.)

[0172] Methods which are well known to those skilled in the art may be used to construct expression vectors containing sequences encoding RMEP and appropriate transcriptional and translational control elements. These methods include in vitro recombinant DNA techniques, synthetic techniques, and in vivo genetic recombination. (See, e.g., Sambrook, J. et al. (1989) Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Press, Plainview N.Y., ch. 4, 8, and 16-17; Ausubel, F. M. et al. (1995) Current Protocols in Molecular Biology, John Wiley & Sons, New York N.Y., ch. 9, 13, and 16.)

[0173] A variety of expression vector/host systems may be utilized to contain and express sequences encoding RMEP. These include, but are not limited to, microorganisms such as bacteria transformed with recombinant bacteriophage, plasmid, or cosmid DNA expression vectors; yeast transformed with yeast expression vectors; insect cell systems infected with viral expression vectors (e.g., baculovirus); plant cell systems transformed with viral expression vectors (e.g., cauliflower mosaic virus, CaMV, or tobacco mosaic virus, TMV) or with bacterial expression vectors (e.g., Ti or pBR322 plasmids); or animal cell systems. (See, e.g., Sambrook, supra; Ausubel, supra; Van Heeke, G. and S. M. Schuster (1989) J. Biol. Chem. 264:5503-5509; Engelhard, E. K. et al. (1994) Proc. Nall. Acad. Sci. USA 91:3224-3227; Sandig, V. et al. (1996) Hum. Gene Ther. 7:1937-1945; Takamatsu, N. (1987) EMBO J. 6:307-311; The McGraw Hill Yearbook of Science and Technology (1992) McGraw Hill, New York N.Y., pp. 191-196; Logan, J. and T. Shenk (1984) Proc. Natl. Acad. Sci. USA 81:3655-3659; and Harrington, J. J. et al. (1997) Nat Genet 15:345-355.) Expression vectors derived from retroviruses, adenoviruses, or herpes or vaccinia viruses, or from various bacterial plasmids, may be used for delivery of nucleotide sequences to the targeted organ, tissue, or cell population. (See, e.g., Di Nicola, M. et al. (1998) Cancer Gen. Ther. 5(6):350-356; Yu, M. et al. (1993) Proc. Natl. Acad. Sci. USA 90(13):6340-6344; Buller, R. M. et al. (1985) Nature 317(6040):813-815; McGregor, D. P. et al. (1994) Mol. Immunol. 31(3):219-226; and Verma, I. M. and N. Somia (1997) Nature 389:239-242.) The invention is not limited by the host cell employed.

[0174] In bacterial systems, a number of cloning and expression vectors may be selected depending upon the use intended for polynucleotide sequences encoding RMEP. For example, routine cloning, subcloning, and propagation of polynucleotide sequences encoding RMEP can be achieved using a multifunctional E. coli vector such as PBLUESCRIPT (Stratagene, La Jolla Calif.) or PSPORT1 plasmid (Life Technologies). Ligation of sequences encoding RMEP into the vector's multiple cloning site disrupts the lacZ gene, allowing a colorimetric screening procedure for identification of transformed bacteria containing recombinant molecules. In addition, these vectors may be usefull for in vitro transcription, dideoxy sequencing, single strand rescue with helper phage, and creation of nested deletions in the cloned sequence. (See, e.g., Van Heeke, G. and S. M. Schuster (1989) J. Biol. Chem. 264:5503-5509.) When large quantities of RMEP are needed, e.g. for the production of antibodies, vectors which direct high level expression of RMEP may be used. For example, vectors containing the strong, inducible SP6 or T7 bacteriophage promoter may be used

[0175] Yeast expression systems may be used for production of RMEP. A number of vectors containing constitutive or inducible promoters, such as alpha factor, alcohol oxidase, and PGH promoters, may be used in the yeast Saccharomyces cerevisiae or Pichia ipastoris. In addition, such vectors direct either the secretion or intracellular retention of expressed proteins and enable integration of foreign sequences into the host genome for stable propagation. (See, e.g., Ausubel, 1995, suora; Bitter, G. A. et al. (1987) Methods Enzymol. 153:516-544; and Scorer, C. A. et al. (1994) Bio/Technology 12:181-184.)

[0176] Plant systems may also be used for expression of RMEP. Transcription of sequences encoding RMEP may be driven by viral promoters, e.g., the 35S and 19S promoters of CaMV used alone or in combination withthe omega leader sequence from TMV (Takamatsu, N. (1987) EMBO J. 6:307-311). Alternatively, plant promoters such as the small subunit of RUBISCO or heat shock promoters may be used. (See, e.g., Coruzzi, G. et al. (1984) EMBO J. 3:1671-1680; Broglie, R. et al. (1984) Science 224:838-843; and Winter, J. et al. (1991) Results Probl. Cell Differ. 17:85-105.) These constructs can be introduced into plant cells by direct DNA transformation or pathogen-mediated transfection: (See, e.g., The McGraw Hill Yearbook of Science and Technology (1992) McGraw Hill, New York N.Y., pp. 191-196.)

[0177] In mammalian cells, a number of viral-based expression systems may be utilized. In cases where an adenovirus is used as an expression vector, sequences encoding RMEP may be ligated into an adenovirus transcription/translation complex consisting of the late promoter and tripartite leader sequence. Insertion in a non-essential E1 or E3 region of the viral genome may be used to obtain infective virus which expresses RMEP inhost cells. (See, e.g., Logan, J. and T. Shenk (1984) Proc. Natl. Acad Sci. USA 81:3655-3659.) In addition, transcription enhancers, such as the Rous sarcoma virus (RSV) enhancer, may be used to increase expression in mammalian host cells. SV40 or EBV-based vectors may also be used for high-level protein expression.

[0178] Human artificial chromosomes (HACs) may also be employed to deliver larger fragments of DNA tan can be contained in and expressed from a plasmid. HACs of about 6 kb to 10 Mb are constructed and delivered via conventional delivery methods (liposomes, polycationic amino polymers, or vesicles) for therapeutic purposes. (See, e.g., Harrington, J. J. et al. (1997) Nat Genet. 15:345-355.)

[0179] For long term production of recombinant proteins in mammalian systems, stable expression of RMEP in cell lines is preferred. For example, sequences encoding RMEP can be transformed into cell lines using expression vectors which may contain viral origins of replication and/or endogenous expression elements and a selectable marker gene on the same or on a separate vector. Following the introduction of the vector, cells may be allowed to grow for about 1 to 2 days in enriched media before being switched to selective media. The purpose of the selectable marker is to confer resistance to a selective agent, and its presence allows growth and recovery of cells which successfully express the introduced sequences. Resistant clones of stably transformed cells may be propagated using tissue culture techniques appropriate to the cell type.

[0180] Any number of selection systems may be used to recover transformed cell lines. These include, but are not limited to, the herpes simplex virus thymidine kinase and adenine phosphoribosyltransferase genes, for use in tk⁻ and apr⁻ cells, respectively. (See, e.g., Wigler, M. et al. (1977) Cell 11:223-232; Lowy, I. et al. (1980) Cell 22:817-823.) Also, antimetabolite, antibiotic, or herbicide resistance can be used as the basis for selection For example, dhfr confers resistance to methotrexate; neo confers resistance to the aminoglycosides neomycin and G-418; and als and pat confer resistance to chlorsuluron and phosphinotricin acetyltransferase, respectively. (See, e.g., Wigler, M. et al. (1980) Proc. Natl. Acad Sci. USA 77:3567-3570; Colbere-Garapin, F. et al. (1981) J. Mol. Biol. 150:1-14.) Additional selectable genes have been described, e.g., trpB and hisD, which alter cellular requirements for metabolites. (See, e.g., Harlman, S. C. and R. C. Mulligan (1988) Proc. Natl. Acad. Sci. USA 85:8047-8051.) Visible markers, e.g., anthocyanins, green fluorescent proteins (GFP; Clontech), β glucuronidase and its substrate β-glucuronide, or luciferase and its substrate luciferin may be used. These markers can be used not only to identify transformants, but also to quantify the amount of transient or stable protein expression attributable to a specific vector system (See, e.g., Rhodes, C. A. (1995) Methods Mol. Biol. 55:121-131.)

[0181] Although the presence/absence of marker gene expression suggests that the gene of interest is also present, the presence and expression of the gene may need to be confirmed. For example, if the sequence encoding RMEP is inserted within a marker gene sequence, transformed cells containing sequences encoding RMEP can be identified by the absence of marker gene function. Alternatively, a marker gene can be placed in tandem with a sequence encoding RMEP under the control of a single promoter. Expression of the marker gene in response to induction or selection usually indicates expression of the tandem gene as well.

[0182] In general, host cells that contain the nucleic acid sequence encoding RMEP and that express RMEP may be identified by a variety of procedures known to those of skill in the art. These procedures include, but are not limited to, DNA-DNA or DNA-RNA hybridizations, PCR amplification, and protein bioassay or immunoassay techniques which include membrane, solution, or chip based technologies for the detection and/or quantification of nucleic acid or protein sequences.

[0183] Immunological methods for detecting and measuring the expression of RMEP using either specific polyclonal or monoclonal antibodies are known in the art. Examples of such techniques include enzyme-linked immunosorbent assays (ELISAs), radioimmunoassays (RIAs), and fluorescence activated cell sorting (FACS). A two-site, monoclonal-based immunoassay utilizing monoclonal antibodies reactive to two non-interfering epitopes on RMEP is preferred, but a competitive binding assay may be employed. These and other assays are well known in the art. (See, e.g., Hampton, R. et al. (1990) Serological Methods, a Laboratory Manual, APS Press, St. Paul Minn., Sect. IV; Coigan, J. E. et al. (1997) Current Protocols in Immunology, Greene Pub. Associates and Wiley-Interscience, New York N.Y.; and Pound, J. D. (1998) Immunochemical Protocols, Humana Press, Totowa N.J.)

[0184] A wide variety of labels and conjugation techniques are known by those skilled in the art and may be used in various nucleic acid and amino acid assays. Means for producing labeled hybridization or PCR probes for detecting sequences related to polynucleotides encoding RMEP include oligolabeling, nick translation, end-labeling, or PCR amplification using a labeled nucleotide. Alternatively, the sequences encoding RMEP, or any fragments thereof, may be cloned into a vector for the production of an mRNA probe. Such vectors are known in the art, are commercially available, and may be used to synthesize RNA probes in vitro by addition of an appropriate RNA polymerase such as T7, T3, or SP6 and labeled nucleotides. These procedures may be conducted using a variety of commercially available kits, such as those provided by Amersham Pharmacia Biotech, Promega (Madison WI), and US Biochemical. Suitable reporter molecules or labels which may be used for ease of detection include radionuclides, enzymes, fluorescent, chemiluminescent, or chromogenic agents, as well as substrates, cofactors, inhibitors, magnetic particles, and the like.

[0185] Host cells transformed with nucleotide sequences encoding RMEP may be cultured under conditions suitable for the expression and recovery of the protein from cell culture. The protein produced by a transformed cell may be secreted or retained intracellularly depending on the sequence and/or the vector used As will be understood by those of skill in the art, expression vectors containing polynucleotides which encode RMEP may be designed to contain signal sequences which direct secretion of RMEP through a prokaryotic or eukaryotic cell membrane.

[0186] In addition, a host cell strain may be chosen for its ability to modulate expression of the inserted sequences or to process the expressed protein in the desired fashion. Such modifications of the polypeptide include, but are not limited to, acetylation, carboxylation, glycosylation, phosphorylation, lipidation, and acylation. Post-translational processing which cleaves a “prepro” or “pro” form of the protein may also be used to specify protein targeting, folding, and/or activity. Different host cells which have specific cellular machinery and characteristic mechanisms for post-translational activities (e.g., CHO, HeLa, MDCK, EK293, and WI38) are available from the American Type Culture Collection (ATCC, Manassas Va.) and may be chosen to ensure the correct modification and processing of the foreign protein.

[0187] In another embodiment of the invention, natural, modified, or recombinant nucleic acid sequences encoding RMEP may be ligated to a heterologous sequence resulting in translation of a fusion protein in any of the aforementioned host systems. For example, a chimeric RMEP protein containing a heterologous moiety that can be recognized by a commercially available antibody may facilitate the screening of peptide libraries for inhibitors of RMEP activity. Heterologous protein and peptide moieties may also facilitate purification of fusion proteins using commercially available affinity matrices. Such moieties include, but are not limited to, glutathione S-transferase (GST), maltose binding protein (MBP), thioredoxin (Trx), calmodulin binding peptide (CBP), 6-His, FLAG, c-myc, and hemagglutin (HA). GST, MBP, Trx, CBP, and 6-His enable purification of their cognate fusion proteins on immobilized glutathione, maltose, phenylarsine oxide, calmodulin, and metal-chelate resins, respectively. FLAG, c-myc, and hemagglutinin (HA) enable immunoaffinity purification of fusion proteins using commercially available monoclonal and polyclonal antibodies that specifically recognize these epitope tags. A fusion protein may also be engineered to contain a proteolytic cleavage site located between the RMEP encoding sequence and the heterologous protein sequence, so that RMEP may be cleaved away from the heterologous moiety following purification. Methods for fusion protein expression and purification are discussed in Ausubel (1995, supra, ch. 10). A variety of commercially available kits may also be used to facilitate expression and purification of fusion proteins.

[0188] In a further embodiment of the invention, synthesis of radiolabeled RMEP may be achieved in vitro using the TNT rabbit reticulocyte lysate or wheat germ extract system (Promega). These systems couple transcription and translation of protein-coding sequences operably associated with the T7, T3, or SP6 promoters. Translation takes place in the presence of a radiolabeled amino acid precursor, for example, ³⁵S-methionine.

[0189] RMEP of the present invention or fragments thereof may be used to screen for compounds that specifically bind to RMEP. At least one and up to a plurality of test compounds may be screened for specific binding to RMEP. Examples of test compounds include antibodies, oligonucleotides, proteins (e.g., receptors), or small molecules.

[0190] In one embodiment, the compound thus identified is closely related to the natural ligand of RMEP, e.g., a ligand or fragment thereof, a natural substrate, a structural or functional mimetic, or a natural binding partner. (See, e.g., Coligan, J. E. et al. (1991) Current Protocols in Immunology 1(2): Chapter 5.) Similarly, the compound can be closely related to the natural receptor to which RMEP binds, or to at least a fragment of the receptor, e.g., the ligand binding site. In either case, the compound can be rationally designed using known techniques. In one embodiment, screening for these compounds involves producing appropriate cells which express RMEP, either as a secreted protein or on the cell membrane. Preferred cells include cells from mammals, yeast, Drosophila, or E. coli. Cells expressing RMEP or cell membrane fractions which contain RMEP are then contacted with a test compound and binding, stimulation, or inhibition of activity of either RMEP or the compound is analyzed.

[0191] An assay may simply test binding of a test compound to the polypeptide, wherein binding is detected by a fluorophore, radioisotope, enzyme conjugate, or other detectable label. For example, the assay may comprise the steps of combining at least one test compound with RMEP, either in solution or affixed to a solid support, and detecting the binding of RMEP to the compound. Alternatively, the assay may detect or measure binding of a test compound in the presence of a labeled competitor. Additionally, the assay may be carried out using cell-free preparations, chemical libraries, or natural product mixtures, and the test compound(s) may be free in solution or affixed to a solid support.

[0192] RMEP of the present invention or fragments thereof may be used to screen for compounds that modulate the activity of RMEP. Such compounds may include agonists, antagonists, or partial or inverse agonists. In one embodiment, an assay is performed under conditions permissive for RMEP activity, wherein RMEP is combined with at least one test compound, and the activity of RMEP in the presence of a test compound is compared with the activity of RMEP in the absence of the test compound. A change in the activity of RMEP in the presence of the test compound is indicative of a compound that modulates the activity of RMEP. Alternatively, a test compound is combined with an in vitro or cell-free system comprising RMEP under conditions suitable for RMEP activity, and the assay is performed. In either of these assays, a test compound which modulates the activity of RMEP may do so indirectly and need not come in direct contact with the test compound. At least one and up to a plurality of test compounds may be screened.

[0193] In another embodiment, polynucleotides encoding RMEP or their mammalian homologs may be “knocked out” in an animal model system using homologous recombination in embryonic stem (ES) cells. Such techniques are well known in the art and are useful for the generation of animal models of human disease. (See, e.g., U.S. Pat. Nos. 5,175,383 and 5,767,337.) For example, mouse ES cells, such as the mouse 129/SvJ cell line, are derived from the early mouse embryo and grown in culture. The ES cells are transformed with a vector containing the gene of interest disrupted by a marker gene, e.g., the neomycin phosphotransferase gene (neo; Capecchi, M. R. (1989) Science 244:1288-1292). The vector integrates into the corresponding region of the host genome by homologous recombination. Alternatively, homologous recombination takes place using the Cre-loxP system to knockout a gene of interest in a tissue- or developmental stage-specific manner (Marth, J. D. (1996) Clin. Invest. 97:1999-2002; Wagner, K. U. et al. (1997) Nucleic Acids Res. 25:4323-4330). Transformed ES cells are identified and microinjected into mouse cell blastocysts such as those from the C57BL/6 mouse strain. The blastocysts are surgically transferred to pseudopregnant dams, and the resulting chimeric progeny are genotyped and bred to produce heterozygous or homozygous strains. Transgenic animals thus generated may be tested with potential therapeutic or toxic agents.

[0194] Polynucleotides encoding RMEP may also be manipulated in vitro in ES cells derived from human blastocysts. Human ES cells have the potential to differentiate into at least eight separate cell lineages including endoderm, mesoderm, and octodermal cell types. These cell lineages differentiate into, for example, neural cells, hematopoietic lineages, and cardiomyocytes (Thomson, J. A. et al. (1998) Science 282:1145-1147).

[0195] Polynucleotides encoding RMEP can also be used to create “knockin” humanized animals (pigs) or transgenic animals (mice or rats) to model human disease. With knockin technology, a region of a polynucleotide encoding RMEP is injected into animal ES cells, and the injected sequence integrates into the animal cell genome. Transformed cells are injected into blastulae, and the blastulae are implanted as described above. Transgenic progeny or inbred lines are studied and treated with potential pharmaceutical agents to obtain information on treatment of a human disease. Alternatively, a mammal inbred to overexpress RMEP, e.g., by secreting RMEP in its milk, may also serve as a convenient source of that protein (Janne, J. et al. (1998) Biotechnol. Annu. Rev. 4:55-74).

[0196] Therapeutics

[0197] Chemical and structural similarity, e.g., in the context of sequences and motifs, exists between regions of RMEP and RNA metabolism proteins. In addition, the expression of RMEP is closely associated with diseased, proliferative, tumorous, and nervous tissues, adrenal tissue, brain tumor tissue, fetal colon tissue, adult colon tissue, prostate epithelial tissue, lymph node cancer tissue, ovarian tissue, pancreatic tissue, and fetal spleen tissue, as well as with diseases of the lung, and physiological conditions that result in anoxia. Therefore, RMEP appears to play a role in nervous system, autoimmune/inflammatory, cell proliferative, and developmental disorders, as well as neoplasms involving lung-specific tissues. In the treatment of disorders associated with increased RMEP expression or activity, it is desirable to decrease the expression or activity of RMEP. In the treatment of disorders associated with decreased RMEP expression or activity, it is desirable to increase the expression or activity of RMEP.

[0198] Therefore, in one embodiment, RMEP or a fragment or derivative thereof may be administered to a subject to treat or prevent a disorder associated with decreased expression or activity of RMEP. Examples of such disorders include, but are not limited to, a nervous system disorder such as epilepsy, ischemic cerebrovascular disease, stroke, cerebral neoplasms, Alzheimer's disease, Pick's disease, Huntington's disease, dementia, Parkinson's disease and other extrapyramidal disorders, amyotrophic lateral sclerosis and other motor neuron disorders, progressive neural muscular atrophy, retinitis pigmentosa, hereditary ataxias, multiple sclerosis and other demyelinating diseases, bacterial and viral meningitis, brain abscess, subdural empyema, epidural abscess, suppurative intracranial thrombophlebitis, myelitis and radiculitis, viral central nervous system disease; prion diseases including kuru, Creutzfeldt-Jakob disease, and Gerstmann-Straussler-Scheinker syndrome; fatal familial insomnia, nutritional and metabolic diseases of the nervous system, neurofibromatosis, tuberous sclerosis, cerebelloretinal hemangioblastomatosis, encephalotrigeminal syndrome, mental retardation and other developmental disorder of the central nervous system, cerebral palsy, a neuroskeletal disorder, an autonomic nervous system disorder, a cranial nerve disorder, a spinal cord disease, muscular dystrophy and other neuromuscular disorder, a peripheral nervous system disorder, dermatomyositis and polymyositis; inherited, metabolic, endocrine, and toxic myopathy; myasthenia gravis, periodic paralysis; a mental disorder including mood, anxiety, and schizophrenic disorders; seasonal affective disorder (SAD); akathesia, amnesia, catatonia, diabetic neuropathy, tardive dyskinesia, dystonias, paranoid psychoses, postherpetic neuralgia, and Tourette's disorder; an autoimmune/inflammatory disorder such as acquired immunodeficiency syndrome (AIDS), Addison's disease, adult respiratory distress syndrome, allergies, ankylosing spondylitis, amyloidosis, anemia, asthma, atherosclerosis, autoimmune hemolytic anemia, autoimmune thyroiditis, autoimmune polyenodocrinopathy-candidiasis-ectodermal dystrophy (APECED), bronchitis, cholecystitis, contact dermatitis, Crohn's disease, atopic dermatitis, dermatomyositis, diabetes mellitus, emphysema, episodic lymphopenia with lymphocytotoxins, erythroblastosis fetalis, erythema nodosum, atrophic gastritis, glomerulonephritis, Goodpasture's syndrome, gout, Graves' disease, Hashimoto's thyroiditis, hypereosinophilia, irritable bowel syndrome, multiple sclerosis, myasthenia gravis, myocardial or pericardial inflammation, osteoarthritis, osteoporosis, pancreatitis, polymyositis, psoriasis, Reiter's syndrome, rheumatoid arthritis, scleroderma, Sjögren's syndrome, systemic anaphylaxis, systemic lupus erythematosus, systemic sclerosis, thrombocytopenic purpura, ulcerative colitis, uveitis, Werner syndrome, complications of cancer, hemodialysis, and extracorporeal circulation, viral, bacterial, fungal, parasitic, protozoal, and helminthic infections, and trauma; a cell proliferative disorder such as actinic keratosis, arteriosclerosis, atherosclerosis, bursitis, cirrhosis, hepatitis, mixed connective tissue disease (MCTD), myelofibrosis, paroxysmal noctura hemoglobinuria, polycythemia vera, psoriasis, primary thrombocythemia, and cancers including adenocarcinoma, leukemia, lymphoma, melanoma, myeloma, sarcoma, teratocarcinoma, and, in particular, cancers of the adrenal gland, bladder, bone, bone marrow, brain, breast, cervix, gall bladder, ganglia, gastrointestinal tract, heart, kidney, liver, lung, muscle, ovary, pancreas, parathyroid, penis, prostate, salivary glands, skin, spleen, testis, thymus, thyroid, and uterus, and a developmental disorder such as renal tubular acidosis, anemia, Cushing's syndrome, achondroplastic dwarfism, Duchenne and Becker muscular dystrophy, epilepsy, gonadal dysgenesis, WAGR syndrome (Wilis' tumor, aniridia, genitourinary abnormalities, and mental retardation), Smith-Magenis syndrome, myclodysplastic syndrome, hereditary mucoepithelial dysplasia, hereditary keratodermas, hereditary neuropathies such as Charcot-Marie-Tooth disease and neurofibromatosis, hypothyroidism, hydrocephalus, seizure disorders such as Syndenham's chorea and cerebral palsy, spina bifida, anencephaly, craniorachischisis, congenital glaucoma, cataract, and sensorineural hearing loss.

[0199] In another embodiment, a vector capable of expressing RMEP or a fragment or derivative thereof may be administered to a subject to treat or prevent a disorder associated with decreased expression or activity of RMEP including, but not limited to, those described above.

[0200] In a further embodiment, a composition comprising a substantially purified RMEP in conjunction with a suitable pharmaceutical carrier may be administered to a subject to treat or prevent a disorder associated with decreased expression or activity of RMEP including, but not limited to, those provided above.

[0201] In still another embodiment, an agonist which modulates the activity of RMEP may be administered to a subject to treat or prevent a disorder associated with decreased expression or activity of RMEP including, but not limited to, those listed above.

[0202] In a further embodiment, an antagonist of RMEP may be administered to a subject to treat or prevent a disorder associated with increased expression or activity of RMEP. Examples of such disorders include, but are not limited to, those nervous system, autoimmune/inflamnatory, cell proliferative, and developmental described above. In one aspect, an antibody which specifically binds RMEP may be used directly as an antagonist or indirectly as a targeting or delivery mechanism for bringing a pharmaceutical agent to cells or tissues which express RMEP.

[0203] In an additional embodiment, a vector expressing the complement of the polynucleotide encoding RMEP may be administered to a subject to treat or prevent a disorder associated with increased expression or activity of RMEP including, but not limited to, those descnred above.

[0204] In other embodiments, any of the proteins, antagonists, antibodies, agonists, complementary sequences, or vectors of the invention may be administered in combination with other appropriate therapeutic agents. Selection of the appropriate agents for use in combination therapy may be made by one of ordinary skill in the art, according to conventional pharmaceutical principles. The combination of therapeutic agents may act synergistically to effect the treatment or prevention of the various disorders described above. Using this approach, one may be able to achieve therapeutic efficacy with lower dosages of each agent, thus reducing the potential for adverse side effects.

[0205] An antagonist of RMEP may be produced using methods which are generally known in the art. In particular, purified RMEP may be used to produce antibodies or to screen libraries of pharmaceutical agents to identify those which specifically bind RMEP. Antibodies to RMEP may also be generated using methods that are well known in the art. Such antibodies may include, but are not limited to, polyclonal, monoclonal, chimeric, and single chain antibodies, Fab fragments, and fragments produced by a Fab expression library. Neutralizing antibodies (i.e., those which inhibit dimer formation) are generally preferred for therapeutic use.

[0206] For the production of antibodies, various hosts including goats, rabbits, rats, mice, humans, and others may be immunized by injection with RMEP or with any fragment or oligopeptide thereof which has immunogenic properties. Depending on the host species, various adjuvants may be used to increase immunological response. Such adjuvants include, but are not limited to, Freund's, mineral gels such as aluminum hydroxide, and surface active substances such as lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, KLH, and dinitrophenol. Among adjuvants used in humans, BCG (bacilli Calmette-Guerin) and Corynebacterium parvum are especially preferable.

[0207] It is preferred that the oligopeptides, peptides, or fragments used to induce antibodies to RMEP have an amino acid sequence consisting of at least about 5 amino acids, and generally will consist of at least about 10 amino acids. It is also preferable that these oligopeptides, peptides, or fragments are identical to a portion of the amino acid sequence of the natural protein. Short stretches of RMEP amino acids may be fused with those of another protein, such as KLH, and antibodies to the chimeric molecule may be produced

[0208] Monoclonal antibodies to RMEP may be prepared using any technique which provides for the production of antibody molecules by continuous cell lines in culture. These include, but are not limited to, the hybridoma technique, the human B-cell hybridoma technique, and the EBV-hybridoma technique. (See, e.g., Kohler, G. et al. (1975) Nature 256:495-497; Kozbor, D. et al. (1985) J. Immunol. Methods 81:31-42; Cote, R. J. et al. (1983) Proc. Natl. Acad Sci. USA 80:2026-2030; and Cole, S. P. et al. (1984) Mol. Cell Biol. 62:109-120.)

[0209] In addition, techniques developed for the production of “chimeric antibodies,” such as the splicing of mouse antibody genes to human antibody genes to obtain a molecule with appropriate antigen specificity and biological activity, can be used. (See, e.g., Morrison, S. L. et al. (1984) Proc. Natl. Acad. Sci. USA 81:6851-6855; Neuberger, M. S. et al. (1984) Nature 312:604-608; and Takeda, S. et al. (1985) Nature 314:452-454.) Alternatively, techniques described for the production of single chain antibodies may be adapted, using methods known in the art, to produce RMEP-specific single chain antibodies. Antibodies with related specificity, but of distinct idiotypic composition, may be generated by chain shuffling from random combinatorial immunoglobulin libraries. (See, e.g., Burton, D. R. (1991) Proc. Natl. Acad. Sci. USA 88:10134-10137.)

[0210] Antibodies may also be produced by inducing in vivo production in the lymphocyte population or by screening immunoglobulin libraries or panels of highly specific binding reagents as disclosed in the literature. (See, e.g., Orlandi, R. et al. (1989) Proc. Natl. Acad. Sci. USA 86:3833-3837; Winter, G. et al. (1991) Nature 349:293-299.)

[0211] Antibody fragments which contain specific binding sites for RMEP may also be generated. For example, such fragments include, but are not limited to, F(ab′)₂ fragments produced by pepsin digestion of the antibody molecule and Fab fragments generated by reducing the disulfide bridges of the F(ab′)2 fragments. Alternatively, Fab expression libraries may be constructed to allow rapid and easy identification of monoclonal Fab fragments with the desired specificity. (See, e.g., Huse, W. D. et al. (1989) Science 246:1275-1281.)

[0212] Various immunoassays may be used for screening to identify antibodies having the desired specificity. Numerous protocols for competitive binding or immunoradiometric assays using either polyclonal or monoclonal antibodies with established specificities are well known in the art. Such immunoassays typically involve the measurement of complex formation between RMEP and its specific antibody. A two-site, monoclonal-based immunoassay utilizing monoclonal antibodies reactive to two non-interfering RMEP epitopes is generally used, but a competitive binding assay may also be employed (Pound, supra).

[0213] Various methods such as Scatchard analysis in conjunction with radioimmunoassay techniques may be used to assess the affinity of antibodies for RMEP. Affinity is expressed as an association constant, K_(a), which is defined as the molar concentration of RMEP-antibody complex divided by the molar concentrations of free antigen and free antibody under equilibrium conditions. The K_(a) determined for a preparation of polyclonal antibodies, which are heterogeneous in their affinities for multiple RMEP epitopes, represents the average affinity, or avidity, of the antibodies for RMEP. The K_(a) determined for a preparation of monoclonal antibodies, which are monospecific for a particular RMEP epitope, represents a true measure of affinity. High-affinity antibody preparations with K_(a) ranging from about 10⁹ to 10¹² L/mole are preferred for use in immunoassays in which the RMEP-antibody complex must withstand rigorous manipulations. Low-affinity antibody preparations with K_(a) ranging from about 10⁶ to 10⁷ L/mole are preferred for use in immunopurification and similar procedures which ultimately require dissociation of RMEP, preferably in active form, from the antibody (Catty, D. (1988) Antibodies, Volume I: A Practical Approach, IRL Press, Washington D.C.; Liddell, J. E. and A. Cryer (1991) A Practical Guide to Monoclonal Antibodies, John Wiley & Sons, New York N.Y.).

[0214] The titer and avidity of polyclonal antibody preparations may be further evaluated to determine the quality and suitability of such preparations for certain downstream applications. For example, a polyclonal antibody preparation containing at least 1-2 mg specific antibody/ml, preferably 5-10 mg specific antibody/ml, is generally employed in procedures requiring precipitation of RMEP-antibody complexes. Procedures for evaluating antibody specificity, titer, and avidity, and guidelines for antibody quality and usage in various applications, are generally available. (See, e.g., Catty, supra, and Coligan et al. supra.)

[0215] In another embodiment of the invention, the polynucleotides encoding RMEP, or any fragment or complement thereof, may be used for therapeutic purposes. In one aspect, modifications of gene expression can be achieved by designing complementary sequences or antisense molecules (DNA, RNA, PNA, or modified oligonucleotides) to the coding or regulatory regions of the gene encoding RMEP. Such technology is well known in the art, and antisense oligonucleotides or larger fragments can be designed from various locations along the coding or control regions of sequences encoding RMEP. (See, e.g., Agrawal, S., ed. (1996) Antisense Therapeutics, Humana Press Inc., Totawa N.J.)

[0216] In therapeutic use, any gene delivery system suitable for introduction of the antisense sequences into appropriate target cells can be used. Antisense sequences can be delivered intracellularly in the form of an expression plasmid which, upon transcription, produces a sequence complementary to at least a portion of the cellular sequence encoding the target protein. (See, e.g., Slater, J. E. et al. (1998) J. Allergy Cli. Immunol. 102(3):469-475; and Scanlon, K. J. et al. (1995) 9(13):1288-1296.) Antisense sequences can also be introduced intracellularly through the use of viral vectors, such as retrovirus and adeno-associated virus vectors. (See, e.g., Miller, A. D. (1990) Blood 76:271; Ausubel, supra; Uckert, W. and W. Walther (1994) Pharmacol. Ther. 63 (3):323-347.) Other gene delivery mechanisms include liposome-derived systems, artificial viral envelopes, and other systems known in the art. (See, e.g., Rossi, J. J. (1995) Br. Med. Bull. 51 (l):217-225; Boado, R. J. et al. (1998) J. Pharm. Sci. 87 (11):1308-1315; and Morris, M. C. et al. (1997) Nucleic Acids Res. 25(14):2730-2736.)

[0217] In another embodiment of the invention, polynucleotides encoding RMEP may be used for somatic or germline gene therapy. Gene therapy may be performed to (i) correct a genetic deficiency (e.g., in the cases of severe combined immunodeficiency (SCID)-X1 disease characterized by X-linked inheritance (Cavazzana-Calvo, M. et al. (2000) Science 288:669-672), severe combined immunodeficiency syndrome associated with an inherited adenosine deaminase (ADA) deficiency (Blaese, R. M. et al. (1995) Science 270:475-480; Bordignon, C. et al. (1995) Science 270:470-475), cystic fibrosis (Zabner, J. et al. (1993) Cell 75:207-216; Crystal, R. G. et al. (1995) Hum. Gene Therapy 6:643-666; Crystal, R. G. et al. (1995) Hum. Gene Therapy 6:667-703), thalassamias, familial hypercholesterolemia, and hemophilia resulting from Factor VIII or Factor IX deficiencies (Crystal, R. G. (1995) Science 270:404-410; Verma, I. M. and N. Somia (1997) Nature 389:239-242)), (ii) express a conditionally lethal gene product (e.g., in the case of cancers which result from unregulated cell proliferation), or (iii) express a protein which affords protection against intracellular parasites (e.g., against human retroviruses, such as human immunodeficiency virus (IRV) (Baltimore, D. (1988) Nature 335:395-396; Poeschla, E. et al. (1996) Proc. Natl. Acad. Sci. USA. 93:11395-11399), hepatitis B or C virus (HBV, HCV); fungal parasites, such as Candida albicans and Paracoccidioides brasillensis; and protozoan parasites such as Plasmodium falciparum and Trypanosoma cruz). In the case where a genetic deficiency in RMEP expression or regulation causes disease, the expression of RMEP from an appropriate population of transduced cells may alleviate the clinical manifestations caused by the genetic deficiency.

[0218] In a further embodiment of the invention, diseases or disorders caused by deficiencies in RMEP are treated by constructing mammalian expression vectors encoding RMEP and introducing these vectors by mechanical means into RMEP-deficient cells. Mechanical transfer technologies for use with cells in vivo or ex vitro include (i) direct DNA microinjection into individual cells, (ii) ballistic gold particle delivery, (iii) liposome-mediated transfection, (iv) receptor-mediated gene transfer, and (v) the use of DNA transposons (Morgan, R. A. and W. F. Anderson (1993) Annu. Rev. Biochem. 62:191-217; Ivics, Z. (1997) Cell 91:501-510; Boulay, J-L. and H. Récipon (1998) Curr. Opin. Biotechnol. 9:445-450).

[0219] Expression vectors that may be effective for the expression of RMEP include, but are not limited to, the PcDNA 3.1, EPITAG, PRCCMV2, PREP, PVAX vectors (Invitrogen, Carlsbad Calif.), PCMV-SCRIPT, PCMV-TAG, PEGSH/PERV (Stratagene, La Jolla Calif.), and PTET-OFF, PTET-ON, PTRE2, PTRE2-LUC, PTK-HYG (Clontech, Palo Alto Calif.). RMEP may be expressed using (i) a constitutively active promoter, (e.g., from cytomegalovirus (CMV), Rous sarcoma virus (RSV), SV40 virus, thymidine kinase (TK), or β-actin genes), (ii) an inducible promoter (e.g., the tetracycline-regulated promoter (Gossen, M. and H. Bujard (1992) Proc. Natl. Acad Sci. USA 89:5547-5551; Gossen, M. et al. (1995) Science 268:1766-1769; Rossi, F. M. V. and H. M. Blau (1998) Curr. Opin. Biotechnol. 9:451-456), commercially available in the T-REX plasmid (nivitrogen)); the ecdysone-inducible promoter (available in the plasmids PVGRXR and PIND; Invitrogen); the FK506/rapamycin inducible promoter; or the RU486/mifepristone inducible promoter (Rossi F. M. V. and Blau, H. M. supra)), or (iii) a tissue-specific promoter or the native promoter of the endogenous gene encoding RMEP from a normal individual.

[0220] Commercially available liposome transformation kits (e.g., the PERFECT LIPID TRANSFECTION KIT, available from Invitrogen) allow one with ordinary skill in the art to deliver polynucleotides to target cells in culture and reuire minimal effort to optimize experimental parameters. In the alternative, transformation is performed using the calcium phosphate method (Graham, F. L. and A. J. Eb (1973) Virology 52:456-467), or by electroporation (Neumann, E. et al. (1982) EMBO J. 1:841-845). The introduction of DNA to primary cells requires modification of these standardized mammallan transfection protocols.

[0221] In another embodiment of the invention, diseases or disorders caused by genetic defects with respect to RMEP expression are treated by constructing a retrovirus vector consisting of (i) the polynucleotide encoding RMEP under the control of an independent promoter or the retrovirus long terminal repeat (LTR) promoter, (ii) appropriate RNA packaging signals, and (mii) a Rev-responsive element (RRE) along with additional retrovirus cis-acting RNA sequences and coding sequences required for efficient vector propagation. Retrovirus vectors (e.g., PFB and PFBNEO) are commercially available (Stratagene) and are based on published data (Riviere, I. et al. (1995) Proc. Natl. Acad. Sci. USA 92:6733-6737), incorporated by reference herein. The vector is propagated in an appropriate vector producing cell line (VPCL) that expresses an envelope gene with a tropism for receptors on the target cells or a promiscuous envelope protein such as VSVg (Armentano, D. et al. (1987) J. Virol. 61:1647-1650; Bender, M. A. et al. (1987) J. Virol. 61:1639-1646; Adam, M. A. and A. D. Miller (1988) J. Virol. 62:3802-3806; Dull, T. et al. (1998) J. Virol. 72:8463-8471; Zufferey, R. et al. (1998) J. Virol. 72:9873-9880). U.S. Pat. No. 5,910,434 to Rigg (“Method for obtaining retrovirus packaging cell lines producing high transducing efficiency retroviral supernatant”) discloses a method for obtaining retrovirus packaging cell lines and is hereby incorporated by reference. Propagation of retrovirus vectors, transduction of a population of cells (e.g., CD4⁺ T-cells), and the return of transduced cells to a patient are procedures well known to persons skilled in the art of gene therapy and have been well documented (Ranga, U. et al. (1997) J. Virol. 71:7020-7029; Bauer, G. et al. (1997) Blood 89:2259-2267; Bonyhadi, M. L. (1997) J. Virol. 71:4707-4716; Ranga, U. et al. (1998) Proc. Natl. Acad. Sci. USA 95:1201-1206; Su, L. (1997) Blood 89:2283-2290).

[0222] In the alternative, an adenovirus-based gene therapy delivery system is used to deliver polynucleotides encoding RMEP to cells which have one or more genetic abnormalities with respect to the expression of RMEP. The construction and packaging of adenovirus-based vectors are well known to those with ordinary skill in the art. Replication defective adenovirus vectors have proven to be versatile for importing genes encoding immunoregulatory proteins into intact islets in the pancreas (Csete, M. E. et al. (1995) Transplantation 27:263-268). Potentially useful adenoviral vectors are described in U.S. Pat. No. 5,707,618 to Armentano (“Adenovirus vectors for gene therapy”), hereby incorporated by reference. For adenoviral vectors, see also Antinozzi, P. A. et al. (1999) Annu. Rev. Nutr. 19:511-544 and Verma, I. M. and N. Somia (1997) Nature 18:389:239-242, both incorporated by reference herein.

[0223] In another alternative, a herpes-based, gene therapy delivery system is used to deliver polynucleotides encoding RMEP to target cells which have one or more genetic abnormalities with respect to the expression of RMEP. The use of herpes simplex virus (HSV)-based vectors may be especially valuable for introducing RMEP to cells of the central nervous system, for which HSV has a tropism. The construction and packaging of herpes-based vectors are well known to those with ordinary skill in the art. A replication-competent herpes simplex virus (HSV) type 1-based vector has been used to deliver a reporter gene to the eyes of primates (Liu, X. et al. (1999) Exp. Eye Res. 169:385-395). The construction of a HSV-1 virus vector has also been disclosed in detail in U.S. Pat. No. 5,804,413 to DeLuca (“Herpes simplex virus strains for gene transfer”), which is hereby incorporated by reference. U.S. Pat. No. 5,804,413 teaches the use of recombinant HSV d92 which consists of a genome containing at least one exogenous gene to be transferred to a cell under the control of the appropriate promoter for purposes including human gene therapy. Also taught by this patent are the construction and use of recombinant HSV strains deleted for ICP4, ICP27 and ICP22. For HSV vectors, see also Goins, W. F. et al. (1999) J. Virol. 73:519-532 and Xu, H. et al. (1994) Dev. Biol. 163:152-161, hereby incorporated by reference. The manipulation of cloned herpesvirus sequences, the generation of recombinant virus following the transfection of multiple plasmids containing different segments of the large herpesvirus genomes, the growth and propagation of herpesvirus, and the infection of cells with herpesvirus are techniques well known to those of ordinary skill in the art.

[0224] In another alternative, an alphavirus (positive, single-stranded RNA virus) vector is used to deliver polynucleotides encoding RMEP to target cells. The biology of the prototypic alphavirus, Semliki Forest Virus (SFV), has been studied extensively and gene transfer vectors have been based on the SFV genome (Garoff, H. and K.-J. Li (1998) Curr. Opin. Biotechnol. 9:464 -469). During alphavirus RNA replication, a subgenomic RNA is generated that normally encodes the viral capsid proteins. This subgenomic RNA replicates to higher levels than the full length genoiic RNA, resulting in the overproduction of capsid proteins relative to the viral proteins with enzymatic activity (e.g., protease and polymerase). Similarly, inserting the coding sequence for RMEP into the alphavirus genome in place of the capsid-coding region results in the production of a large number of RMEP-coding RNAs and the synthesis of high levels of RMEP in vector transduced cells. Wbile alphavirus infection is typically associated with cell lysis within a few days, the ability to establish a persistent infection in hamster normal kidney cells (BHK-21) with a variant of Sindbis virus (SIN) indicates that the lytic replication of alphaviruses can be altered to suit the needs of the gene therapy application (Dryga, S. A et al. (1997) Virology 228:7483). The wide host range of alphaviruses will allow the introduction of RMEP into a variety of cell types. The specific transduction of a subset of cells in a population may require the sorting of cells prior to transduction. The methods of manipulating infectious cDNA clones of alphaviruses, performing alphavirus cDNA and RNA transfections, and performing alphavirus infections, are well known to those with ordinary skill in the art

[0225] Oligonucleotides derived from the transcription initiation site, e.g., between about positions −10 and +10 from the start site, may also be employed to inhibit gene expression. Similarly, inhibition can be achieved using triple helix base-pairing methodology. Triple helix pairing is useful because it causes inhibition of the ability of the double helix to open sufficiently for the binding of polymerases, transcription factors, or regulatory molecules. Recent therapeutic advances using triplex DNA have been described in the literature. (See, e.g., Gee, J. E. et al. (1994) in Huber, B. E. and B. I. Carr, Molecular and Immunologic Approaches, Future Publishing, Mt. Kisco N.Y., pp. 163-177.) A complementary sequence or antisense molecule may also be designed to block translation of mRNA by preventing the transcript from binding to ribosomes.

[0226] Ribozymes, enzymatic RNA molecules, may also be used to catalyze the specific cleavage of RNA. The mechanism of ribozyme action involves sequence-specific hybridization of the ribozyme molecule to complementary target RNA, followed by endonucleolytic cleavage. For example, engineered hammerhead motif ribozyme molecules may specifically and efficiently catalyze endonucleolytic cleavage of sequences encoding RMEP.

[0227] Specific ribozyme cleavage sites within any potential RNA target are initially identified by scanning the target molecule for ribozyme cleavage sites, including the following sequences: GUA, GUU, and GUC. Once identified, short RNA sequences of between 15 and 20 ribonucleotides, corresponding to the region of the target gene containing the cleavage site, may be evaluated for secondary structural features which may render the oligonucleotide inoperable. The suitability of candidate targets may also be evaluated by testing accessibility to hybridization with complementary oligonucleotides using ribonuclease protection assays.

[0228] Complementary ribonucleic acid molecules and ribozymes of the invention may be prepared by any method known in the art for the synthesis of nucleic acid molecules. These include techniques for chemically synthesizing oligonucleotides such as solid phase phosphoramidite chemical synthesis. Alternatively, RNA molecules may be generated by in vitro and in vivo transcription of DNA sequences encoding RMEP. Such DNA sequences may be incorporated into a wide variety of vectors with suitable RNA polymerase promoters such as T7 or SP6. Alternatively, these cDNA constructs that synthesize complementary RNA, constitutively or inducibly, can be introduced into cell lines, cells, or tissues.

[0229] RNA molecules may be modified to increase intracellular stability and half-life. Possible modifications include, but are not limited to, the addition of flanking sequences at the 5′ and/or 3′ ends of the molecule, or the use of phosphorothioate or 2′ O-methyl rather than phosphodiesterase linkages within the backbone of the molecule. This concept is inherent in the production of PNAs and can be extended in all of these molecules by the inclusion of nontraditional bases such as inosine, queosine, and wybutosine, as well as acetyl-, methyl-, thio-, and similarly modified forms of adenine, cytidine, guamine, thymine, and uridine which are not as easily recognized by endogenous endonucleases.

[0230] An additional embodiment of the invention encompasses a method for screening for a compound which is effective in altering expression of a polynucleotide encoding RMEP. Compounds which may be effective in altering expression of a specific polynucleotide may include, but are not limited to, oligonucleotides, antisense oligonucleotides, triple helix-forming ohigonucleotides, transcription factors and other polypeptide transcriptional regulators, and non-macromolecular chemical entities which are capable of interacting with specific polynucleotide sequences. Effective compounds may alter polynucleotide expression by acting as either inhibitors or promoters of polynucleotide expression. Thus, in the treatment of disorders associated with increased RMEP expression or activity, a compound which specifically inhibits expression of the polynucleotide encoding RMEP may be therapeutically usefuil, and in the treatment of disorders associated with decreased RMEP expression or activity, a compound which specifically promotes expression of the polynucleotide encoding RMEP may be therapeutically useful.

[0231] At least one, and up to a plurality, of test compounds may be screened for effectiveness in altering expression of a specific polynucleotide. A test compound may be obtained by any method commonly known in the art, including chemical modification of a compound known to be effective in altering polynucleotide expression; selection from an existing, commercially-available or proprietary library of naturally-occurring or non-natural chemical compounds; rational design of a compound based on chemical and/or structural properties of the target polynucleotide; and selection from a library of chemical compounds created combinatorially or randomly. A sample comprising a polynucleotide encoding RMEP is exposed to at least one test compound thus obtained. The sample may comprise, for example, an intact or permeability cell, or an in vitro cell-free or reconstituted biochemical system. Alterations in the expression of a polynucleotide encoding RMEP are assayed by any method commonly known in the art. Typically, the expression of a specific nucleotide is detected by hybridization with a probe having a nucleotide sequence complementary to the sequence of the polynucleotide encoding RMEP. The amount of hybridization may be quantified, thus forming the basis for a comparison of the expression of the polynucleotide both with and without exposure to one or more test compounds. Detection of a change in the expression of a polynucleotide exposed to a test compound indicates that the test compound is effective in altering the expression of the polynucleotide. A screen for a compound effective in altering expression of a specific polynucleotide can be carried out, for example, using a Schizosaccharomyces pombe gene expression system (Atkins, D. et al. (1999) U.S. Pat. No. 5,932,435; Arndt, G. M. et al. (2000) Nucleic Acids Res. 28:E15) or a human cell line such as HeLa cell (Clarke, M. L. et al. (2000) Biochem. Biophys. Res. Commun. 268:8-13). A particular embodiment of the present invention involves screening a combinatorial library of oligonucleotides (such as deoxyribonucleotides, ribonucleotides, peptide nucleic acids, and modified oligonucleotides) for antisense activity against a specific polynucleotide sequence (Bruice, T. W. et al. (1997) U.S. Pat. No. 5,686,242; Bruice, T. W. et al. (2000) U.S. Pat. No. 6,022,691).

[0232] Many methods for introducing vectors into cells or tissues are available and equally suitable for use in vivo, in vitro, and ex vivo. For ex vivo therapy, vectors may be introduced into stem cells taken from the patient and clonally propagated for autologous transplant back into that same patient. Delivery by transfection, by liposome injections, or by polycationic amino polymers may be achieved using methods which are well known in the art. (See, e.g., Goldman, C. K. et al. (1997) Nat. Biotechnol. 15:462-466.)

[0233] Any of the therapeutic methods described above may be applied to any subject in need of such therapy, including, for example, mammals such as humans, dogs, cats, cows, horses, rabbits, and monkeys.

[0234] An additional embodiment of the invention relates to the administration of a composition which generally comprises an active ingredient formulated with a pharmaceutically acceptable excipient Excipients may include, for example, sugars, starches, celluloses, gums, and proteins. Various formulations are commonly known and are thoroughly discussed in the latest edition of Remington's Pharmaceutical Sciences (Maack Publishing, Easton Pa.). Such compositions may consist of RMEP, antibodies to RMEP, and mimetics, agonists, antagonists, or inhibitors of RMEP.

[0235] The compositions utilized in this invention may be administered by any number of routes including, but not limited to, oral, intravenous, intramuscular, intra-arterial, intramedullary, intrathecal, intraventricular, pulmonary, transdermal, subcutaneous, intraperitoneal, intranasal, enteral, topical, sublingual, or rectal means.

[0236] Compositions for pulmonary administration may be prepared in liquid or dry powder form. These compositions are generally aerosolized immediately prior to inhalation by the patient. In the case of small molecules (e.g. traditional low molecular weight organic drugs), aerosol delivery of fast-acting formulations is well-known in the art. In the case of macromolecules (e.g. larger peptides and proteins), recent developments in the field of pulmonary delivery via the alveolar region of the lung have enabled the practical delivery of drugs such as insulin to blood circulation (see, e.g., Patton, J. S. et al., U.S. Pat. No. 5,997,848). Pulmonary delivery has the advantage of administration without needle injection, and obviates the need for potentially toxic penetration enhancers.

[0237] Compositions suitable for use in the invention include compositions wherein the active ingredients are contained in an effective amount to achieve the intended purpose. The determination of an effective dose is well within the capability of those skilled in the art.

[0238] Specialized forms of compositions may be prepared for direct intracellular delivery of macromolecules comprising RMEP or fragments thereof. For example, liposome preparations containing a cell-impermeable macromolecule may promote cell fusion and intracellular delivery of the macromolecule. Alternatively, RMEP or a fragment thereof may be joined to a short cationic N-terminal portion from the HIV Tat-1 protein. Fusion proteins thus generated have been found to transduce into the cells of all tissues, including the brain, in a mouse model system (Schwarze, S. R. et al. (1999) Science 285:1569-1572).

[0239] For any compound, the therapeutically effective dose can be estimated initially either in cell culture assays, e.g., of neoplastic cells, or in animal models such as mice, rats, rabbits, dogs, monkeys, or pigs. An animal model may also be used to determine the appropriate concentration range and route of administration. Such information can then be used to determine useful doses and routes for administration in humans.

[0240] A therapeutically effective dose refers to that amount of active ingredient, for example RMEP or fragments thereof, antibodies of RMEP, and agonists, antagonists or inhibitors of RMEP, which ameliorates the symptoms or condition. Therapeutic efficacy and toxicity may be determined by standard pharmaceutical procedures in cell cultures or with experimental animals, such as by calculating the ED₅₀ (the dose therapeutically effective in 50% of the population) or LD₅₀ (the dose lethal to 50% of the population) statistics. The dose ratio of toxic to therapeutic effects is the therapeutic index, which can be expressed as the LD₅₀/ED₅₀ ratio. Compositions which exhibit large therapeutic indices are preferred. The data obtained from cell culture assays and animal studies are used to formulate a range of dosage for human use. The dosage contained in such compositions is preferably within a range of circulating concentrations that includes the ED₅₀ with little or no toxicity. The dosage varies within this range depending upon the dosage form employed, the sensitivity of the patient, and the route of administration.

[0241] The exact dosage will be determined by the practitioner, in light of factors related to the subject requiring treatment. Dosage and administration are adjusted to provide sufficient levels of the active moiety or to maintain the desired effect. Factors which may be taken into account include the severity of the disease state, the general health of the subject, the age, weight, and gender of the subject, time and frequency of administration, drug combination(s), reaction sensitivities, and response to therapy. Long-acting compositions may be administered every 3 to 4 days, every week, or biweekly depending on the half-life and clearance rate of the particular formulation.

[0242] Normal dosage amounts may vary from about 0.1 μg to 100,000 μg, up to a total dose of about 1 gram, depending upon the route of administration. Guidance as to particular dosages and methods of delivery is provided in the literature and generally available to practitioners in the art. Those skilled in the art will employ different formulations for nucleotides than for proteins or their inhibitors. Similarly, delivery of polynucleotides or polypeptides will be specific to particular cells, conditions, locations, etc.

[0243] Diagnostics

[0244] In another embodiment, antibodies which specifically bind RMEP may be used for the diagnosis of disorders characterized by expression of RMEP, or in assays to monitor patients being treated with RMEP or agonists, antagonists, or inhibitors of RMEP. Antibodies useful for diagnostic purposes may be prepared in the same manner as described above for therapeutics. Diagnostic assays for RMEP include methods which utilize the antibody and a label to detect RMEP in human body fluids or in extracts of cells or tissues. The antibodies may be used with or without modification, and may be labeled by covalent or non-covalent attachment of a reporter molecule. A wide variety of reporter molecules, several of which are described above, are known in the art and may be used.

[0245] A variety of protocols for measuring RMEP, including ELISAs, RIAs, and FACS, are known in the art and provide a basis for diagnosing altered or abnormal levels of RMEP expression. Normal or standard values for RMEP expression are established by combining body fluids or cell extracts taken from normal mammalian subjects, for example, human subjects, with antibodies to RMEP under conditions suitable for complex formation. The amount of standard complex formation may be quantitated by various methods, such as photometric means. Quantities of RMEP expressed in subject, control, and disease samples from biopsied tissues are compared with the standard values. Deviation between standard and subject values establishes the parameters for diagnosing disease.

[0246] In another embodiment of the invention, the polynucleotides encoding RMEP may be used for diagnostic purposes. The polynucleotides which may be used include oligonucleotide sequences, complementary RNA and DNA molecules, and PNAs. The polynucleotides may be used to detect and quantify gene expression in biopsied tissues in which expression of RMEP may be correlated with disease. The diagnostic assay may be used to determine absence, presence, and excess expression of RMEP, and to monitor regulation of RMEP levels during therapeutic intervention.

[0247] In one aspect, hybridization with PCR probes which are capable of detecting polynucleotide sequences, including genomic sequences, encoding RMEP or closely related molecules may be used to identify nucleic acid sequences which encode RMEP. The specificity of the probe, whether it is made from a highly specific region, e.g., the 5′ regulatory region, or from a less specific region, e.g., a conserved motif, and the stringency of the hybridization or amplification will determine whether the probe identifies only naturally occurring sequences encoding RMEP, acelic variants, or related sequences.

[0248] Probes may also be used for the detection of related sequences, and may have at least 50% sequence identity to any of the RMEP encoding sequences. The hybridization probes of the subject invention may be DNA or RNA and may be derived from the sequence of SEQ ID NO:48-94 or from genomic sequences including promoters, enhancers, and introns of the RMEP gene.

[0249] Means for producing specific hybridization probes for DNAs encoding RMEP include the cloning of polynucleotide sequences encoding RMEP or RMEP derivatives into vectors for the production of mRNA probes. Such vectors are known in the art, are commercially available, and may be used to synthesize RNA probes in vitro by means of the addition of the appropriate RNA polymerases and the appropriate labeled nucleotides. Hybridization probes may be labeled by a variety of reporter groups, for example, by radionuclides such as ³²p or ³⁵S, or by enzymatic labels, such as alkaline phosphatase coupled to the probe via avidin/biotin coupling systems, and the like.

[0250] Polynucleotide sequences encoding RMEP may be used for the diagnosis of disorders associated with expression of RMEP. Examples of such disorders include, but are not limited to, a nervous system disorder such as epilepsy, ischemic cerebrovascular disease, stroke, cerebral neoplasms, Alzheimer's disease, Pick's disease, Huntington's disease, dementia, Parkinson's disease and other extrapyramidal disorders, amyotrophic lateral sclerosis and other motor neuron disorders, progressive neural muscular atrophy, retinitis pigmentosa, hereditary ataxias, multiple sclerosis and other demyelinating diseases, bacterial and viral meningitis, brain abscess, subdural empyema, epidural abscess, suppurative intracranial thrombophlebitis, myelitis and radiculitis, viral central nervous system disease; prion diseases including kuru, Creutzfeldt-Jakob disease, and Gerstmann-Straussler-Scheinker syndrome; fatal familial insomnia, nutritional and metabolic diseases of the nervous system, neurofibromatosis, tuberous sclerosis, cerebelloretinal hemangioblastomatosis, encephalotrigeminal syndrome, mental retardation and other developmental disorder of the central nervous system, cerebral palsy, a neuroskeletal disorder, an autonomic nervous system disorder, a cranial nerve disorder, a spinal cord disease, muscular dystrophy and other neuromuscular disorder, a peripheral nervous system disorder, dermatomyositis and polymyositis; inherited, metabolic, endocrine, and toxic myopathy; myasthenia gravis, periodic paralysis; a mental disorder including mood, anxiety, and schizophrenic disorders; seasonal affective disorder (SAD); akathesia, amnesia, catatonia, diabetic neuropathy, tardive dyslinesia, dystonias, paranoid psychoses, postherpetic neuralgia, and Tourette's disorder; an autoimmune/inflammatory disorder such as acquired immunodeficiency syndrome (AIDS), Addison's disease, adult respiratory distress syndrome, allergies, ankylosing spondylitis, amyloidosis, anemia, asthma, atherosclerosis, autoinmune hemolytic anemia, autoimmune thyroiditis, autoimmune polyenodocrinopathy-candidiasis-ectodermal dystrophy (APECED), bronchitis, cholecystitis, contact dermatitis, Crohn's disease, atopic dermatitis, dermatomyositis, diabetes melrntus, emphysema, episodic lymphopenia with lymphocytotoxins, erythroblastosis fetalis, erythema nodosum, atrophic gastritis, glomerulonephritis, Goodpasture's syndrome, gout, Graves' disease, Hashinioto's thyroiditis, hypereosinophilia, irritable bowel syndrome, multiple sclerosis, myasthenia gravis, myocardial or pericardial inflammation, osteoartbritis, osteoporosis, pancreatitis, polymyositis, psoriasis, Reiter's syndrome, rheumatoid arthritis, sclerodenma, Sjögren's syndrome, systemic anaphylaxis, systemic lupus erythematosus, systemic sclerosis, thrombocytopenic purpura, ulcerative colitis, uveitis, Werner syndrome, complications of cancer, hemodialysis, and extracorporeal circulation, viral, bacterial, fungal, parasitic, protozoal, and helminthic infections, and trauma; a cell proliferative disorder such as actinic keratosis, arteriosclerosis, atherosclerosis, bursitis, cirrhosis, hepatitis, mixed connective tissue disease (MCTD), myelofibrosis, paroxysmal nocturnal hemoglobinuria, polycythemia vera, psoriasis, primary thrombocythemia, and cancers including adenocarcinoma, leukemia, lymphoma, melanoma, myeloma, sarcoma, teratocarcinoma, and, in particular, cancers of the adrenal gland, bladder, bone, bone marrow, brain, breast, cervix, gall bladder, ganglia, gastrointestinal tract, heart, kidney, liver, lung, muscle, ovary, pancreas, parathyroid, penis, prostate, salivary glands, skin, spleen, testis, thymus, thyroid, and uterus, and a developmental disorder such as renal tubular acidosis, anemia, Cushing's syndrome, achondroplastic dwarfism, Duchenne and Becker muscular dystrophy, epilepsy, gonadal dysgenesis, WAGR syndrome (Wilms' tumor, aniridia, genitourinary abnormalities, and mental retardation), Smith-Magenis syndrome, myelodysplastic syndrome, hereditary mucoepithelial dysplasia, hereditary keratodermas, hereditary neuropathies such as Charcot-Marie-Tooth disease and neurofibromatosis, hypothyroidism, hydrocephalus, seizure disorders such as Syndenham's chorea and cerebral palsy, spina bifida, anencephaly, craniorachischisis, congenital glaucoma, cataract, and sensorineural hearing loss. The polynucleotide sequences encoding RMEP may be used in Southern or northern analysis, dot blot, or other membrane-based technologies; in PCR technologies; in dipstick, pin, and multiformat ELISA-like assays; and in microarrays utilizing fluids or tissues from patients to detect altered RMEP expression. Such qualitative or quantitative methods are well known in the art.

[0251] In a particular aspect, the nucleotide sequences encoding RMEP may be useful in assays that detect the presence of associated disorders, particularly those mentioned above. The nucleotide sequences encoding RMEP may be labeled by standard methods and added to a fluid or tissue sample from a patient under conditions suitable for the formation of hybridization complexes. After a suitable incubation period, the sample is washed and the signal is quantified and compared with a standard value. If the amount of signal in the patient sample is significantly altered in comparison to a control sample then the presence of altered levels of nucleotide sequences encoding RMEP in the sample indicates the presence of the associated disorder. Such assays may also be used to evaluate the efficacy of a particular therapeutic treatment regimen in animal studies, in clinical trials, or to monitor the treatment of an individual patient.

[0252] In order to provide a basis for the diagnosis of a disorder associated with expression of RMEP, a normal or standard profile for expression is established. This may be accomplished by combining body fluids or cell extracts taken from normal subjects, either animal or human, with a sequence, or a fragment thereof, encoding RMEP, under conditions suitable for hybridization or amplification. Standard hybridization may be quantified by comparing the values obtained from normal subjects with values from an experiment in which a known amount of a substantially purified polynucleotide is used Standard values obtained in this manner may be compared with values obtained from samples from patients who are symptomatic for a disorder. Deviation from standard values is used to establish the presence of a disorder.

[0253] Once the presence of a disorder is established and a treatment protocol is initiated, hybridization assays may be repeated on a regular basis to determine if the level of expression in the patient begins to approximate that which is observed in the normal subject. The results obtained from successive assays may be used to show the efficacy of treatment over a period ranging from several days to months.

[0254] With respect to cancer, the presence of an abnormal amount of transcript (either under- or overexpressed) in biopsied tissue from an individual may indicate a predisposition for the development of the disease, or may provide a means for detecting the disease prior to the appearance of actual clinical symptoms. A more definite diagnosis of this type may allow health professionals to employ preventative measures or aggressive treatment earlier thereby preventing the development or further progression of the cancer.

[0255] Additional diagnostic uses for oligonucleotides designed from the sequences encoding RMEP may involve the use of PCR. These oligomers may be chemically synthesized, generated enzymatically, or produced in vitro. Oligomers will preferably contain a fragment of a polynucleotide encoding RMEP, or a fragment of a polynucleotide complementary to the polynucleotide encoding RMEP, and will be employed under optimized conditions for identification of a specific gene or condition. Oligomers may also be employed under less stringent conditions for detection or quantification of closely related DNA or RNA sequences.

[0256] In a particular aspect, oligonucleotide primers derived from the polynucleotide sequences encoding RMEP may be used to detect single nucleotide polymorphisms (SNPs). SNPs are substitutions, insertions and deletions that are a frequent cause of inherited or acquired genetic disease in humans. Methods of SNP detection include, but are not limited to, singlestranded conformation polymorphism (SSCP) and fluorescent SSCP (fSSCP) methods. In SSCP, oligonucleotide primers derived from the polynucleotide sequences encoding RMEP are used to amplify DNA using the polymerase chain reaction (PCR). The DNA may be derived, for example, from diseased or normal tissue, biopsy samples, bodily fluids, and the lime. SNPs in the DNA cause differences in the secondary and tertiary structures of PCR products in single-stranded form, and these differences are detectable using gel electrophoresis in non-denaturing gels. In fSCCP, the oligonucleotide primers are fluorescently labeled, which allows detection of the amplimers in high-throughput equipment such as DNA sequencing machines. Additionally, sequence database analysis methods, termed in silico SNP (isSNP), are capable of identifying polymorphisms by comparing the sequence of individual overlapping DNA fragments which assemble into a common consensus sequence. These computer-based methods filter out sequence variations due to laboratory preparation of DNA and sequencing errors using statistical models and automated analyses of DNA sequence chromatogram. In the alternative, SNPs may be detected and characterized by mass spectrometry using, for example, the high throughput MASSARRAY system (Sequenom, Inc., San Diego Calif.).

[0257] Methods which may also be used to quantify the expression of RMEP include radiolabeling or biotinylating nucleotides, coamplification of a control nucleic acid, and interpolating results from standard curves. (See, e.g., Melby, P. C. et al. (1993) J. Immunol. Methods 159:235-244; Duplaa, C. et al. (1993) Anal. Biochem. 212:229-236.) The speed of quantitation of multiple samples may be accelerated by running the assay in a high-throughput format where the oligomer or polynucleotide of interest is presented in various dilutions and a spectrophotometric or calorimetric response gives rapid quantitation.

[0258] In further embodiments, oligonucleotides or longer fragments derived from any of the polynucleotide sequences described herein may be used as elements on a microarray. The microarray can be used in transcript imaging techniques which monitor the relative expression levels of large numbers of genes simultaneously as described below. The microarray may also be used to identify genetic variants, mutations, and polymorphisms. This information may be used to determine gene function, to understand the genetic basis of a disorder, to diagnose a disorder, to monitor progression/regression of disease as a function of gene expression, and to develop and monitor the activities of therapeutic agents in the treatment of disease. In particular, this information may be used to develop a pharmacogenomic profile of a patient in order to select the most appropriate and effective treatment regimen for that patient. For example, therapeutic agents which are highly effective and display the fewest side effects may be selected for a patient based on his/her pharmacogenomic profile.

[0259] In another embodiment, RMEP, fragments of RMP, or antibodies specific for RMEP may be used as elements on a microarray. The microarray may be used to monitor or measure protein-protein interactions, drug-target interactions, and gene expression profiles, as described above.

[0260] A particular embodiment relates to the use of the polynucleotides of the present invention to generate a transcript image of a tissue or cell type. A transcript image represents the global pattern of gene expression by a particular tissue or cell type. Global gene expression patterns are analyzed by quantifying the number of expressed genes and their relative abundance under given conditions and at a given time. (See Seilhamer et al., “Comparative Gene Transcript Analysis,” U.S. Pat. No. 5,840,484, expressly incorporated by reference herein.) Thus a transcript image may be generated by hybridizing the polynucleotides of the present invention or their complements to the totality of transcripts or reverse transcripts of a particular tissue or cell type. In one embodiment, the hybridization takes place in high-throughput format, wherein the polynucleotides of the present invention or their complements comprise a subset of a plurality of elements on a microarray. The resultant transcript image would provide a profile of gene activity.

[0261] Transcript images may be generated using transcripts isolated from tissues, cell lines, biopsies, or other biological samples. The transcript image may thus reflect gene expression in vivo, as in the case of a tissue or biopsy sample, or in vitro, as in the case of a cell line.

[0262] Transcript images which profile the expression of the polynucleotides of the present invention may also be used in conjunction with in vitro model systems and preclinical evaluation of pharmaceuticals, as well as toxicological testing of industrial and naturally-occurring environmental compounds. All compounds induce characteristic gene expression patterns, frequently termed molecular fingerprints or toxicant signatures, which are indicative of mechanisms of action and toxicity (Nuwaysir, E. F. et al. (1999) Mol. Carcinog. 24:153-159; Steiner, S. and N. L. Anderson (2000) Toxicol. Lett. 112-113:467-471, expressly incorporated by reference herein). If a test compound has a signature similar to that of a compound with known toxicity, it is likely to share those toxic properties. These fingerprints or signatures are most useful and refined when they contain expression information from a large number of genes and gene families. Ideally, a genome-wide measurement of expression provides the highest quality signature. Even genes whose expression is not altered by any tested compounds are important as well, as the levels of expression of these genes are used to normalize the rest of the expression data. The normalization procedure is useful for comparison of expression data after treatment with different compounds. While the assignment of gene function to elements of a toxicant signature aids in interpretation of toxicity mechanisms, knowledge of gene function is not necessary for the statistical matching of signatures which leads to prediction of toxicity. (See, for example, Press Release 00-02 from the National Institute of Environmental Health Sciences, released Feb. 29, 2000, available at http://www.niehs.nih.gov/oc/news/toxchip.htm.) Therefore, it is important and desirable in toxicological screening using toxicant signatures to include all expressed gene sequences.

[0263] In one embodiment, the toxicity of a test compound is assessed by treating a biological sample containing nucleic acids with the test compound. Nucleic acids that are expressed in the treated biological sample are hybridized with one or more probes specific to the polynucleotides of the present invention, so that transcript levels corresponding to the polynucleotides of the present invention may be quantified. The transcript levels in the treated biological sample are compared with levels in an untreated biological sample. Differences in the transcript levels between the two samples are indicative of a toxic response caused by the test compound in the treated sample.

[0264] Another particular embodiment relates to the use of the polypeptide sequences of the present invention to analyze the proteome of a tissue or cell type. The term proteome refers to the global pattern of protein expression in a particular tissue or cell type. Each protein component of a proteome can be subjected individually to further analysis. Proteome expression patterns, or profiles, are analyzed by quantifying the number of expressed proteins and their relative abundance under given conditions and at a given time. A profile of a cell's proteome may thus be generated by separating and analyzing the polypeptides of a particular tissue or cell type. In one embodiment, the separation is achieved using two-dimensional gel electrophoresis, in which proteins from a sample are separated by isoelectric focusing in the first dimension, and then according to molecular weight by sodium dodecyl sulfate slab gel electrophoresis in the second dimension (Steiner and Anderson, supra). The proteins are visualized in the gel as discrete and uniquely positioned spots, typically by staining the gel with an agent such as Coomassie Blue or silver or fluorescent stains. The optical density of each protein spot is generally proportional to the level of the protein in the sample. The optical densities of equivalently positioned protein spots from different samples, for example, from biological samples either treated or untreated with a test compound or therapeutic agent, are compared to identity any changes in protein spot density related to the treatment The proteins in the spots are partially sequenced using, for example, standard methods employing chemical or enzymatic cleavage followed by mass spectrometry. The identity of the protein in a spot may be determined by comparing its partial sequence, preferably of at least 5 contiguous amino acid residues, to the polypeptide sequences of the present invention. In some cases, further sequence data may be obtained for definitive protein identification

[0265] A proteomic profile may also be generated using antibodies specific for RMEP to quantify the levels of RMEP expression. In one embodiment, the antibodies are used as elements on a microarray, and protein expression levels are quantified by exposing the microarray to the sample and detecting the levels of protein bound to each array element (Lueling, A. et al. (1999) Anal. Biochem. 270:103-111; Mendoze, L. G. et al. (1999) Biotechniques 27:778-788). Detection may be performed by a variety of methods known in the art, for example, by reacting the proteins in the sample with a thiol- or amino-reactive fluorescent compound and detecting the amount of fluorescence bound at each array element.

[0266] Toxicant signatures at the proteome level are also usefull for toxicological screening, and should be analyzed in parallel with toxicant signatures at the transcript level. There is a poor correlation between transcript and protein abundances for some proteins in some tissues (Anderson, N. L. and J. Seilhamer (1997) Electrophoresis 18:533-537), so proteome toxicant signatures may be useful in the analysis of compounds which do not significantly affect the transcript image, but which alter the proteomic profile. In addition, the analysis of transcripts in body fluids is difficult, due to rapid degradation of mRNA, so proteomic profiling may be more reliable and informative in such cases.

[0267] In another embodiment, the toxicity of a test compound is assessed by treating a biological sample containing proteins with the test compound. Proteins that are expressed in the treated biological sample are separated so that the amount of each protein can be quantified The amount of each protein is compared to the amount of the corresponding protein in an untreated biological sample. A difference in the amount of protein between the two samples is indicative of a toxic response to the test compound in the treated sample. Individual proteins are identified by sequencing the amino acid residues of the individual proteins and comparing these partial sequences to the polypeptides of the present invention.

[0268] In another embodiment, the toxicity of a test compound is assessed by treating a biological sample containing proteins with the test compound. Proteins from the biological sample are incubated with antibodies specific to the polypeptides of the present invention. The amount of protein recognized by the antibodies is quantified The amount of protein in the treated biological sample is compared with the amount in an untreated biological sample. A difference in the amount of protein between the two, samples is indicative of a toxic response to the test compound in the treated sample.

[0269] Microarrays may be prepared, used, and analyzed using methods known in the art. (See, e.g., Brennan, T. M. et al. (1995) U.S. Pat. No. 5,474,796; Schena, M. et al. (1996) Proc. Natl. Acad. Sci. USA 93:10614-10619; Baldeschweiler et al. (1995) PCT application WO95/251116; Shalon, D. et al. (1995) PCT application WO95/35505; Heller, R. A. et al. (1997) Proc. Natl. Acad. Sci. USA 94:2150-2155; and Heller, M. J. et al. (1997) U.S. Pat. No. 5,605,662.) Various types of microarrays are well known and thoroughly described in DNA Microarrays: A Practical Approach, M. Schena, ell (1999) Oxford University Press, London, hereby expressly incorporated by reference.

[0270] In another embodiment of the invention, nucleic acid sequences encoding RMEP may be used to generate hybridization probes useful in mapping the naturally occurring genomic sequence. Either coding or noncoding sequences may be used, and in some instances, noncoding sequences may be preferable over coding sequences. For example, conservation of a coding sequence among members of a multi-gene family may potentially cause undesired cross hybridization during chromosomal mapping. The sequences may be mapped to a particular chromosome, to a specific region of a chromosome, or to artificial chromosome constructions, e.g., human artificial chromosomes (HACs), yeast artificial chromosomes (YACs), bacterial artificial chromosomes (BACs), bacterial P1 constructions, or single chromosome cDNA libraries. (See, e.g., Harrington, J. J. et al. (1997) Nat Genet. 15:345-355; Price, C. M. (1993) Blood Rev. 7:127-134; and Trask, B. J. (1991) Trends Genet. 7:149-154.) Once mapped, the nucleic acid sequences of the invention may be used to develop genetic linkage maps, for example, which correlate the inheritance of a disease state with the inheritance of a particular chromosome region or restriction fragment length polymorphism (RFLP). (See, for example, Lander, E. S. and D. Botstein (1986) Proc. Natl. Acad. Sci. USA 83:7353-7357.)

[0271] Fluorescent in situ hybridization (FISH) may be correlated with other physical and genetic map data. (See, e.g., Heinz-Ulrich, et al. (1995) in Meyers, supra, pp. 965-968.) Examples of genetic map data can be found in various scientific journals or at the Online Mendelian Inheritance in Man (OMIM) World Wide Web site. Correlation between the location of the gene encoding RMEP on a physical map and a specific disorder, or a predisposition to a specific disorder, may help define the region of DNA associated with that disorder and thus may further positional cloning efforts.

[0272] In situ hybridization of chromosomal preparations and physical mapping techniques, such as linkage analysis using established chromosomal markers, may be used for extending genetic maps. Often the placement of a gene on the chromosome of another mammalian species, such as mouse, may reveal associated markers even if the exact chromosomal locus is not known. This information is valuable to investigators searching for disease genes using positional cloning or other gene discovery techniques. Once the gene or genes responsible for a disease or syndrome have been crudely localized by genetic linkage to a particular genomic region, e.g., ataxia-telangiectasia to 11q22-23, any sequences mapping to that area may represent associated or regulatory genes for further investigation. (See, e.g., Gatti, R. A. et al. (1988) Nature 336:577-580.) The nucleotide sequence of the instant invention may also be used to detect differences in the chromosomal location due to translocation, inversion, etc., among normal, carrier, or affected individuals.

[0273] In another embodiment of the invention, RMEP, its catalytic or immunogenic fragments, or oligopeptides thereof can be used for screening libraries of compounds in any of a variety of drug screening techniques. The fragment employed in such screening may be free in solution, affixed to a solid support, borne on a cell surface, or located intracellularly. The formation of binding complexes between RMEP and the agent being tested may be measured.

[0274] Another technique for drug screening provides for high throughput screening of compounds having suitable binding affinity to the protein of interest. (See, e.g., Geysen, et al. (1984) PCT application WO84/03564.) In this method, large numbers of different small test compounds are synthesized on a solid substrate. The test compounds are reacted with RMEP, or fragments thereof, and washed. Bound RMEP is then detected by methods well known in the art. Purified RMEP can also be coated directly onto plates for use in the aforementioned drug screening techniques. Alternatively, non-neutralizing antibodies can be used to capture the peptide and immobilize it on a solid support.

[0275] In another embodiment, one may use competitive drug screening assays in which neutralizing antibodies capable of binding RMEP specifically compete with a test compound for binding RMEP. In this manner, antibodies can be used to detect the presence of any peptide which shares one or more antigenic determinants with RMEP.

[0276] In additional embodiments, the nucleotide sequences which encode RMEP may be used in any molecular biology techniques that have yet to be developed, provided the new techniques rely on properties of nucleotide sequences that are currently known, including, but not limited to, such properties as the triplet genetic code and specific base pair interactions.

[0277] Without further elaboration, it is believed that one skilled in the art can, using the preceding description, utilize the present invention to its fullest extent The following embodiments are, therefore, to be construed as merely illustrative, and not limitative of the remainder of the disclosure in any way whatsoever.

[0278] The disclosures of all patents, applications, and publications mentioned above and below, including U.S. Ser. No. 60/201,875, U.S. Ser. No. 60/200,184, U.S. Ser. No. 60/202,090, U.S. Ser. No. 60/210,232, and U.S. Ser. No. 60/220,553, are hereby expressly incorporated by reference.

EXAMPLES

[0279] I. Construction of cDNA Libraries

[0280] Incyte cDNAs were derived from cDNA libraries described in the LIFESEQ GOLD database (Incyte Genomics, Palo Alto Calif.) and shown in Table 4, column 5. Some tissues were homogenized and lysed in guanidinium isothiocyanate, while others were homogenized and lysed in phenol or in a suitable mixture of denaturants, such as TRIZOL (Life Technologies), a monophasic solution of phenol and guanidine isothiocyanate. The resulting lysates were centrifuged over CsCl cushions or extracted with chloroform RNA was precipitated from the lysates with either isopropanol or sodium acetate and ethanol, or by other routine methods.

[0281] Phenol extraction and precipitation of RNA were repeated as necessary to increase RNA purity. In some cases, RNA was treated with DNase. For most libraries, poly(A)+RNA was isolated using oligo d(T)-coupled paramagnetic particles (Promega), OLIGOTEX latex particles (QIAGEN, Chatsworth Calif.), or an OLIGOTEX mRNA purification kit (QIAGEN). Alternatively, RNA was isolated directly from tissue lysates using other RNA isolation kits, e.g., the POLY(A)PURE mRNA purification kit (Ambion, Austin Tex.).

[0282] In some cases, Stratagene was provided with RNA and constructed the corresponding cDNA libraries. Otherwise, cDNA was synthesized and cDNA libraries were constructed with the UNIZAP vector system (Stratagene) or SUPERSCRIPT plasmid system (Life Technologies), using the recommended procedures or similar methods known in the art. (See, e.g., Ausubel, 1997, supra, units 5.1-6.6.) Reverse transcription was initiated using oligo d(T) or random primers. Synthetic oligonucleotide adapters were ligated to double stranded cDNA, and the cDNA was digested with the appropriate restriction enzyme or enzymes. For most libraries, the cDNA was size-selected (300-1000 bp) using SEPHACRYL S1000, SEPHAROSE CL2B, or SEPHAROSE CL4B column chromatography (Amersham Pharmacia Biotech) or preparative agarose gel electrophoresis. cDNAs were ligated into compatible restriction enzyme sites of the polylinker of a suitable plasmid, e.g., PBLUESCRIPT plasmid (Stratagene), PSPORT1 plasmid (Life Technologies), PCDNA2.1 plasmid (Invitrogen, Carlsbad Calif.), PBK-CMV plasmid (Stratagene), or pINCY (Incyte Genomics, Palo Alto Calif.), or derivatives thereof. Recombinant plasmids were transformed into competent E. coil cells including XL1-Blue, XL1-BlueMRF, or SOLR from Stratagene or DH5α, DH10B, or ElectroMAX DH10B from Life Technologies.

[0283] II. Isolation of cDNA Clones

[0284] Plasmids obtained as described in Example I were recovered from host cells by in vivo excision using the UNIZAP vector system (Stratagene) or by cell lysis. Plasmids were purified using at least one of the following: a Magic or WIZARD Minipreps DNA purification system (Promega); an AGTC Miniprep purification kit (Edge Biosystems, Gaithersburg Md.); and QIAWELL 8 Plasmid, QIAWELL 8 Plus Plasmid, QIAWELL 8 Ultra Plasmid purification systems or the R.E.A.L. PREP 96 plasmid purification kit from QIAGEN. Following precipitation, plasmids were resuspended in 0.1 ml of distilled water and stored, with or without lyophihiation, at 4° C.

[0285] Alternatively, plasmid DNA was amplified from host cell lysates using direct link PCR in a high-throughput format (Rao, V. B. (1994) Anal. Biochem 216:1-14). Host cell lysis and thermal cycling steps were carried out in a single reaction mixture. Samples were processed and stored in 384-well plates, and the concentration of amplified plasmid DNA was quantified fluorometrically using PICOGREEN dye (Molecular Probes, Eugene Oreg.) and a FLUOROSKAN II fluorescence scanner (Labsystems Oy, Helsinki, Finland).

[0286] III. Sequencing and Analysis

[0287] Incyte cDNA recovered in plasmids as described in Example II were sequenced as follows. Sequencing reactions were processed using standard methods or high-throughput instrumentation such as the ABI CATALYST 800 (Applied Biosystems) thermal cycler or the PTC-200 thermal cycler (MJ Research) in conjunction with the HYDRA microdispenser (Robbins Scientific) or the MICROLAB 2200 (Hamilton) liquid transfer system cDNA sequencing reactions were prepared using reagents provided by Amersham Pharmacia Biotech or supplied in ABI sequencing kits such as the ABI PRISM BIGDYE Terminator cycle sequencing ready reaction kit (Applied Biosystems). Electrophoretic separation of cDNA sequencing reactions and detection of labeled polynucleotides were carried out using the MEGABASE 1000 DNA sequencing system (Molecular Dynamics); the ABI PRISM 373 or 377 sequencing system (Applied Biosystems) in conjunction with standard ABI protocols and base calling software; or other sequence analysis systems known in the art. Reading frames within the cDNA sequences were identified using standard methods (reviewed in Ausubel, 1997, supra, unit 7.7). Some of the cDNA sequences were selected for extension using the techniques disclosed in Example VIII.

[0288] The polynucleotide sequences derived from Incyte cDNAs were validated by removing vector, linker, and poly(A) sequences and by masking ambiguous bases, using algorithms and programs based on BLAST, dynamic programming, and dinucleotide nearest neighbor analysis. The Incyte cDNA sequences or translations thereof were then queried against a selection of public databases such as the GenBank primate, rodent, mammalian, vertebrate, and eukaryote databases, and BLOCKS, PRINTS, DOMO, PRODOM, and hidden Markov model (HMM)-based protein family databases such as PFAM. (HMM is a probabilistic approach which analyzes consensus primary structures of gene families. See, for example, Eddy, S. R. (1996) Curr. Opin. Struct. Biol. 6:361-365.) The queries were performed using programs based on BLAST, FASTA, BLIMPS, and HMMER. The Incyte cDNA sequences were assembled to produce full length polynucleotide sequences. Alternatively, GenBank cDNAs, GenBank ESTs, stitched sequences, stretched sequences, or Genscan-predicted coding sequences (see Examples IV and V) were used to extend Incyte cDNA assemblages to full length. Assembly was performed using programs based on Phred, Phrap, and Consed, and cDNA assemblages were screened for open reading frames using programs based on GeneMark, BLAST, and FASTA The full length polynucleotide sequences were translated to derive the corresponding full length polypeptide sequences. Alternatively, a polypeptide of the invention may begin at any of the methionine residues of the fulfl length translated polypeptide. Full length polypeptide sequences were subsequently analyzed by querying against databases such as the GenBank protein databases (genpept), SwissProt, BLOCKS, PRINTS, DOMO, PRODOM, Prosite, and hidden Markov model (HMM)-based protein family databases such as PFAM. Full length polynucleotide sequences are also analyzed using MACDNASIS PRO software (Hitachi Software Engineering, South San Francisco Calif.) and LASERGENE software (DNASTAR). Polynucleotide and polypeptide sequence alignments are generated using default parameters specified by the CLUSTAL algorithm as incorporated into the MEGALIGN multisequence alignment program (DNASTAR), which also calculates the percent identity between aligned sequences.

[0289] Table 7 summarizes the tools, programs, and algorithms used for the analysis and assembly of Incyte cDNA and full length sequences and provides applicable descriptions, references, and threshold parameters. The first column of Table 7 shows the tools, programs, and algorithms used, the second column provides brief descriptions thereof, the third column presents appropriate references, all of which are incorporated by reference herein in their entirety, and the fourth column presents, where applicable, the scores, probability values, and other parameters used to evaluate the strength of a match between two sequences (the higher the score or the lower the probability value, the greater the identity between two sequences).

[0290] The programs described above for the assembly and analysis of full length polynucleotide and polypeptide sequences were also used to identify polynucleotide sequence fragments from SEQ ID NO:48-94. Fragments from about 20 to about 4000 nucleotides which are useful in hybridization and amplification technologies are described in Table 4, column 4.

[0291] IV. Identification and Editing of Coding Sequences from Genonic DNA

[0292] Putative RNA metabolism proteins were initially identified by running the Genscan gene identification program against public genomic sequence databases (e.g., gbpri and gbhtg). Genscan is a general-purpose gene identification program which analyzes genomic DNA sequences from a variety of organisms (See Burge, C. and S. Karlin (1997) J. Mol. Biol. 268:78-94, and Burge, C. and S. Karlin (1998) Curr. Opin. Struct. Biol. 8:346-354). The program concatenates predicted exons to form an assembled cDNA sequence extending from a methionine to a stop codon. The output of Genscan is a FASTA database of polynucleotide and polypeptide sequences. The maximum range of sequence for Genscan to analyze at once was set to 30 kb. To determine which of these Genscan predicted cDNA sequences encode RNA metabolism proteins, the encoded polypeptides were analyzed by querying against PFAM models for RNA metabolism proteins. Potential RNA metabolism proteins were also identified by homology to Incyte cDNA sequences that had been annotated as RNA metabolism proteins. These selected Genscan-predicted sequences were then compared by BLAST analysis to the genpept and gbpri public databases. Where necessary, the Genscan-predicted sequences were then edited by comparison to the top BLAST hit from genpept to correct errors in the sequence predicted by Genscan, such as extra or omitted exons. BLAST analysis was also used to find any Incyte cDNA or public cDNA coverage of the Genscan-predicted sequences, thus providing evidence for transcription. When Incyte cDNA coverage was available, this information was used to correct or confirm the Genscan predicted sequence. Full length polynucleotide sequences were obtained by assembling Genscan-predicted coding sequences with Incyte cDNA sequences and/or public cDNA sequences using the assembly process described in Example III. Alternatively, full length polynucleotide sequences were derived entirely from edited or unedited Genscan-predicted coding sequences.

[0293] V. Assembly of Genomic Sequence Data with cDNA Sequence Data

[0294] “Stretched” Sequences

[0295] Partial cDNA sequences were extended with exons predicted by the Genscan gene identification program described in Example IV. Partial cDNAs assembled as described in Example III were mapped to genomic DNA and parsed into clusters containing related cDNAs and Genscan exon predictions from one or more genomic sequences. Each cluster was analyzed using an algorithm based on graph theory and dynamic programming to integrate cDNA and genomic information, generating possible splice variants that were subsequently confirmed, edited, or extended to create a full length sequence. Sequence intervals in which the entire length of the interval was present on more than one sequence in the cluster were identified, and intervals thus identified were considered to be equivalent by transitivity. For example, if an interval was present on a cDNA and two genomic sequences, then all three intervals were considered to be equivalent This process allows unrelated but consecutive genomic sequences to be brought together, bridged by cDNA sequence. Intervals thus identified were then “stitched” together by the stitching algorithm in the order that they appear along their parent sequences to generate the longest possible sequence, as well as sequence variants. Linkages between intervals which proceed along one type of parent sequence (cDNA to cDNA or genomic sequence to genomic sequence) were given preference over linkages which change parent type (cDNA to genomic sequence). The resultant stitched sequences were translated and compared by BLAST analysis to the genpept and gbpri public databases. Incorrect exons predicted by Genscan were corrected by comparison to the top BLAST hit from genpept. Sequences were further extended with additional cDNA sequences, or by inspection of genomic DNA, when necessary.

[0296] “Stretched” Sequences

[0297] Partial DNA sequences were extended to full length with an algorithm based on BLAST analysis. First, partial cDNAs assembled as described in Example III were queried against public databases such as the GenBank primate, rodent, mammalian, vertebrate, and eukaryote databases using the BLAST program The nearest GenBank protein homolog was then compared by BLAST analysis to either Incyte cDNA sequences or GenScan exon predicted sequences described in Example IV. A chimeric protein was generated by using the resultant high-scoring segment pairs (HSPs) to map the translated sequences onto the GenBank protein homolog. Insertions or deletions may occur in the chimeric protein with respect to the original GenBank protein homolog. The GenBank protein homolog, the chimeric protein, or both were used as probes to search for homologous genomic sequences from the public human genome databases. Partial DNA sequences were therefore “stretched” or extended by the addition of homologous genomic sequences. The resultant stretched sequences were examined to determine whether it contained a complete gene.

[0298] VI. Chromosomal Mapping of RMEP Encoding Polynucleotides

[0299] The sequences which were used to assemble SEQ ID NO:48-94 were compared with sequences from the Incyte LIFESEQ database and public domain databases using BLAST and other implementations of the Smith-Waterman algorithm. Sequences from these databases that matched SEQ ID NO:48-94 were assembled into clusters of contiguous and overlapping sequences using assembly algorithms such as Phrap (Table 7). Radiation hybrid and genetic mapping data available from public resources such as the Stanford Human Genome Center (SHGC), Whitehead Institute for Genome Research (WIGR), and Généthon were used to determine if any of the clustered sequences had been previously mapped. Inclusion of a mapped sequence in a cluster resulted in the assignment of all sequences of that cluster, including its particular SEQ ID NO:, to that map location.

[0300] Map locations are represented by ranges, or intervals, of human chromosomes. The map position of an interval, in centiMorgans, is measured relative to the terminus of the chromosome's p-arm. (The centiMorgan (cM) is a unit of measurement based on recombination frequencies between chromosomal markers. On average, 1 cM is roughly equivalent to 1 megabase (Mb) of DNA in humans, although this can vary widely due to hot and cold spots of recombination.) The cM distances are based on genetic markers mapped by Genethon which provide boundaries for radiation hybrid markers whose sequences were included in each of the clusters. Human genome maps and other resources available to the public, such as the NCBI “GeneMap'99 ” World Wide Web site (http://www.ncbi.nlm.nih.gov/genemap/), can be employed to determine if previously identified disease genes map within or in proximity to the intervals indicated above.

[0301] In this manner, SEQ ID NO:53 was mapped to chromosome 1 within the interval from 159.6 to 164.1 centiMorgans. SEQ ID NO:61 was mapped to chromosome 8 within the interval from 30.70 to 60.00 centiMorgans. SEQ ID NO:69 was mapped to chromosome 10 within the interval from 158.30 centiMorgans to the q terminus. SEQ ID NO:70 was mapped to chromosome 1 within the interval from 63.90 to 74.80 centiMorgans. SEQ ID NO:71 was mapped to chromosome 1 within the interval from 159.60 to 164.10 centiMorgans. SEQ ID NO:73 was mapped to chromosome 11 within the interval from 34.30 to 37.00 centiMorgans. SEQ ID NO:75 was mapped to chromosome 2 within the interval from 107.10 to 118.00 centiMorgans. SEQ ID NO:76 was mapped to chromosome 7 within the interval from 7.80 to 10.60 centiMorgans. SEQ ID NO:79 was mapped to chromosome 22 within the interval from 22.20 to 40.20 centiMorgans. SEQ ID NO:81 was mapped to chromosome 4 within the interval from the p terminus to 6.70 centiMorgans. SEQ ID NO: 84 was mapped to chromosome 5 within the interval from 156.0 to 157.6 centiMorgans. SEQ ID NO: 88 was mapped to chromosome 11 within the interval from 117.9 to 123.5 centiMorgans. SEQ ID NO:91 was mapped to chromosome 5 within the interval from 152.3 to 155.5 centiMorgans.

[0302] VII. Analysis of Polynucleotide Expression

[0303] Northern analysis is a laboratory technique used to detect the presence of a transcript of a gene and involves the hybridization of a labeled nucleotide sequence to a membrane on which RNAs from a particular cell type or tissue have been bound. (See, e.g., Sambrook, supra, ch . 7; Ausubel (1995) supra, ch. 4 and 16.)

[0304] Analogous computer techniques applying BLAST were used to search for identical or related molecules in cDNA databases such as GenBank or LIFESEQ (Incyte Genomics). This analysis is much faster than multiple membrane-based hybridizations. In addition, the sensitivity of the computer search can be modified to determine whether any particular match is categorized as exact or similar. The basis of the search is the product score, which is defined as: $\frac{{BLAST}\quad {Score} \times {P{ercent}}\quad {Identity}}{5 \times {minimum}\quad \left\{ {{{length}\left( {{Seq}.\quad 1} \right)},{{length}\left( {{Seq}.\quad 2} \right)}} \right\}}$

[0305] The product score takes into account both the degree of similarity between two sequences and the length of the sequence match The product score is a normalized value between 0 and 100, and is calculated as follows: the BLAST score is multiplied by the percent nucleotide identity and the product is divided by (5 times the length of the shorter of the two sequences). The BLAST score is calculated by assigning a score of +5 for every base that matches in a high-scoring segment pair (HSP), and −4 for every mismatch. Two sequences may share more than one HSP (separated by gaps). If there is more than one HSP, then the pair with the highest BLAST score is used to calculate the product score. The product score represents a balance between fractional overlap and quality in a BLAST alignment. For example, a product score of 100 is produced only for 100% identity over the entire length of the shorter of the two sequences being compared. A product score of 70 is produced either by 100% identity and 70% overlap at one end, or by 88% identity and 100% overlap at the other. A product score of 50 is produced either by 100% identity and 50% overlap at one end, or 79% identity and 100% overlap.

[0306] Alternatively, polynucleotide sequences encoding RMEP are analyzed with respect to the tissue sources from which they were derived. For example, some full length sequences are assembled, at least in part, with overlapping Incyte cDNA sequences (see Example III). Each cDNA sequence is derived from a cDNA library constructed from a human tissue. Each human tissue is classified into one of the following organ/tissue categories: cardiovascular system; connective tissue; digestive system; embryonic structures; endocrine system; exocrine glands; genitalia, female; genitalia, male; germ cells; hemic and immune system; liver; musculoskeletal system; nervous system; pancreas; respiratory system; sense organs; skin; stomatognathic system; unclassified/mixed; or urinary tract. The number of libraries in each category is counted and divided by the total number of libraries across all categories. Similarly, each human tissue is classified into one of the following disease/condition categories: cancer, cell line, developmental, inflammation, neurological, trauma, cardiovascular, pooled, and other, and the number of libraries in each category is counted and divided by the total number of libraries across all categories. The resulting percentages reflect the tissue- and disease-specific expression of cDNA encoding RMEP. cDNA sequences and cDNA library/tissue information are found in the LIFESEQ GOLD database (Incyte Genomics, Palo Alto Calif.).

[0307] VIII. Extension of RMEP Encoding Polynucleotides

[0308] Full length polynucleotide sequences were also produced by extension of an appropriate fragment of the full length molecule using oligonucleotide primers designed from this fragment. One primer was synthesized to initiate 5′ extension of the known fragment, and the other primer was synthesized to initiate 3′ extension of the known fragment. The initial primers were designed using OLIGO 4.06 software (National Biosciences), or another appropriate program, to be about 22 to 30 nucleotides in length, to have a GC content of about 50% or more, and to anneal to the target sequence at temperatures of about 68° C. to about 72° C. Any stretch of nucleotides which would result in hairpin structures and primer-primer dimerizations was avoided.

[0309] Selected human cDNA libraries were used to extend the sequence. If more than one extension was necessary or desired, additional or nested sets of primers were designed.

[0310] High fidelity amplification was obtained by PCR using methods well known in the art. PCR was performed in 96-well plates using the PTC-200 thermal cycler (MJ Research, Inc.). The reaction mix contained DNA template, 200 nmol of each primer, reaction buffer containing Mg²⁺, (NH₄)₂SO₄, and 2-mercaptoethanol, Taq DNA polymerase (Amersham Pharmacia Biotech), ELONGASE enzyme (Life Technologies), and Pfu DNA polymerase (Stratagene), with the following parameters for primer pair PCI A and PCI B: Step 1: 94° C., 3 min; Step 2: 94° C., 15 sec; Step 3: 60° C., 1 min; Step 4: 68° C., 2 min; Step5: Steps 2, 3, and4 repeated 20 times; Step 6: 68° C., 5 min; Step 7: storage at 4: 68° C. In the alternative, the parameters for primer pair T7 and SK+were as follows: Step 1: 94° C., 3 min; Step 2: 94° C., 15 sec; Step 3: 57° C., 1 min; Step 4: 68° C., 2 min; Step 5: Steps 2, 3, and 4 repeated 20 times; Step 6: 68° C., 5 min; Step 7; storage at 4° C.

[0311] The concentration of DNA in each well was determined by dispensing 100 μl PICOGREEN quantitation reagent (0.25% (v/v) PICOGREEN; Molecular Probes, Eugene Oreg.) dissolved in 1X TE and 0.5 μl of undiluted PCR product into each well of an opaque fluorimeter plate (Caning Costar, Acton Mass.), allowing the DNA to bind to the reagent. The plate was scanned in a Fluoroskan II (Labsystems Oy, Helsinki, Finland) to measure the fluorescence of the sample and to quantify the concentration of DNA. A 5μl to 10 μl aliquot of the reaction mixture was analyzed by electrophoresis on a 1% agarose gel to determine which reactions were successful in extending the sequence.

[0312] The extended nucleotides were desalted and concentrated, transferred to 384-well plates, digested with Civic cholera virus endonuclease (Molecular Biology Research, Madison Wis.), and sonicated or sheared prior to religation into pUC 18 vector (Amersham Pharmacia Biotech). For shotgun sequencing, the digested nucleotides were separated on low concentration (0.6 to 0.8%) agarose gels, fragments were excised, and agar digested with Agar ACE (Promega). Extended clones were religated using T4 ligase (New England Biolabs, Beverly Mass.) into pUC 18 vector (Amersham Pharmacia Biotech), treated with Pfu DNA polymerase (Stratagene) to fill-in restriction site overhangs, and transfected into competent E. coli cells. Transformed cells were selected on antibiotic-containing media, and individual colonies were picked and cultured overnight at 37° C. in 384-well plates in LB/2x carb liquid media.

[0313] The cells were lysed, and DNA was amplified by PCR using Taq DNA polymerase (Amersham Pharmacia Biotech) and Pfu DNA polymerase (Stratagene) with the following parameters: Step 1: 94° C., 3 min; Step 2: 94° C., 15 sec; Step 3: 60° C., 1 min; Step 4: 72° C., 2 min; Step 5: steps 2, 3, and 4 repeated 29 times; Step 6: 72° C., 5 min; Step 7; storage at 4° C. DNA was quantified by PICOGREEN reagent (Molecular Probes) as described above. Samples with low DNA recoveries were reamplified using the same conditions as described above. Samples were diluted with 20% dimethylsulfoxide (1:2, v/v), and sequenced using DYENAMIC energy transfer sequencing primers and the DYENAMIC DIRECT kit (Amersham Pharmacia Biotech) or the ABI PRISM BIGDYE Terminator cycle sequencing ready reaction kit (Applied Biosystems).

[0314] In like manner, full length polynucleotide sequences are verified using the above procedure or are used to obtain 5′ regulatory sequences using the above procedure along with oligonucleotides designed for such extension, and an appropriate genomic library.

[0315] IX. Labeling and Use of Individual Hybridization Probes

[0316] Hybridization probes derived from SEQ ID NO:48-94 are employed to screen cDNAs, genomic DNAs, or mRNAs. Although the labeling of oligonucleotides, consisting of about 20 base pairs, is specifically described, essentially the same procedure is used with larger nucleotide fragments. Oligonucleotides are designed using state-of-the-art software such as OLIGO 4.06 software (National Biosciences) and labeled by combining 50 pmol of each oligomer, 250 μCi of [γ³²P] adenosine triphosphate (Amersham Pharmacia Biotech), and T4 polynucleotide kinase (DuPont NEN, Boston Mass.). The labeled oligonucleotides are substantially purified using a SEPHADEX G-25 superfine size exclusion dextran bead column (Amersham Pharmacia Biotech). An aliquot containing 10⁷ counts per minute of the labeled probe is used in a typical membrane-based hybridization analysis of human genomic DNA digested with one of the following endonucleases: Ase I, Bgl II, Eco RI, Pst I, Xba I, or Pvu II (DuPont NEN).

[0317] The DNA from each digest is fractionated on a 0.7% agarose gel and transferred to nylon membranes (Nytran Plus, Schleicher & Schuell, Durham NH). Hybridization is carried out for 16 hours at 40° C. To remove nonspecific signals, blots are sequentially washed at room temperature under conditions of up to, for example, 0.1×saline sodium citrate and 0.5% sodium dodecyl sulfate. Hybridization patterns are visualized using autoradiography or an alternative imaging means and compared.

[0318] X. Microarrays

[0319] The linkage or synthesis of array elements upon a microarray can be achieved utilizing photolithography, piezoelectric printing (ink-jet printing, See, e.g., Baldeschweiler, supra.), mechanical microspotting technologies, and derivatives thereof. The substrate in each of the aforementioned technologies should be uniform and solid with a non-porous surface (Schena (1999), supra). Suggested substrates include silicon, silica, glass slides, glass chips, and silicon wafers. Alternatively, a procedure analogous to a dot or slot blot may also be used to arrange and link elements to the surface of a substrate using thermal, UV, chemical, or mechanical bonding procedures. A typical array may be produced using available methods and machines well known to those of ordinary skill in the art and may contain any appropriate number of elements. (See, e.g., Schena, M. et al. (1995) Science 270:467-470; Shalon, D. et al. (1996) Genome Res. 6:639-645; Marshall, A. and J. Hodgson (1998) Nat. Biotechnol. 16:27-31.)

[0320] Full length eDNAs, Expressed Sequence Tags (ESTs), or fragments or oligomers thereof may comprise the elements of the microarray. Fragments or oligomers suitable for hybridization can be selected using software well known in the art such as LASERGENE software (DNASTAR). The array elements are hybridized with polynucleotides in a biological sample. The polynucleotides in the biological sample are conjugated to a fluorescent label or other molecular tag for ease of detection. After hybridization, nonhybridized nucleotides from the biological sample are removed, and a fluorescence scanner is used to detect hybridization at each array element. Alternatively, laser desorbtion and mass spectrometry may be used for detection of hybridization. The degree of complementarity and the relative abundance of each polynucleotide which hybridizes to an element on the microarray may be assessed. In one embodiment, microarray preparation and usage is described in detail below.

[0321] Tissue or Cell Sample Preparation

[0322] Total RNA is isolated from tissue samples using the guanidinium thiocyanate method and poly(A)⁺ RNA is purified using the oligo-(dT) cellulose method. Each poly(A)⁺ RNA sample is reverse transcribed using MMLV reverse-transcriptase, 0.05 pg/μl oligo-(dT) primer (21 mer), 1× first strand buffer, 0.03 units/μl RNase inhibitor, 500 μM dATP, 500 μM dGTP, 500 μM dTTP, 40 μM dCTP, 40 μM dCTP-Cy3 (BDS) or dCTP-Cy5 (Amersham Pharmacia Biotech). The reverse transcription reaction is performed in a 25 ml volume containing 200 ng poly(A)⁺ RNA with GEMBRIGHT kits (Incyte). Specific control poly(A)⁺ RNAs are synthesized by in vitro transcription from non-coding yeast genomic DNA. After incubation at 37° C. for 2 hr, each reaction sample (one with Cy3 and another with Cy5 labeling) is treated with 2.5 ml of 0.5 M sodium hydroxide and incubated for 20 minutes at 85° C. to the stop the reaction and degrade the RNA. Samples are purified using two successive CHROMA SPIN 30 gel filtration spin columns (CLONTECH Laboratories, Inc. (CLONTECH), Palo Alto Calif.) and after combining, both reaction samples are ethanol precipitated using 1 ml of glycogen (1 mg/ml), 60 ml sodium acetate, and 300 ml of 100% ethanol. The sample is then dried to completion using a SpeedVAC (Savant Instruments Inc., Holbrook N.Y.) and resuspended in 14μl 5×SSC/0.2% SDS.

[0323] Microarray Preparation

[0324] Sequences of the present invention are used to generate array elements. Each array element is amplified from bacterial cells containing vectors with cloned cDNA inserts. PCR amplification uses primers complementary to the vector sequences flanking the cDNA insert. Array elements are amplified in thirty cycles of PCR from an initial quantity of 1-2 ng to a final quantity greater than 5 μg. Amplified array elements are then purified using SEPHACRYL400 (Amersham Pharmacia Biotech).

[0325] Purified array elements are immobilized on polymer-coated glass slides. Glass microscope slides (Corning) are cleaned by ultrasound in 0.1% SDS and acetone, with extensive distilled water washes between and after treatments. Glass slides are etched in 4% hydrofluoric acid (VWR Scientific Products Corporation (VWR), West Chester Pa.), washed extensively in distilled water, and coated with 0.05% aminopropyl silane (Sigma) in 95% ethanol. Coated slides are cured in a 110° C. oven.

[0326] Array elements are applied to the coated glass substrate using a procedure described in U.S. Pat. No. 5,807,522, incorporated herein by reference. 1 μl of the array element DNA, at an average concentration of 100 ng/μl, is loaded into the open capillary printing element by a high-speed robotic apparatus. The apparatus then deposits about 5 nl of array element sample per slide.

[0327] Microarrays are UV-crosslinked using a STRATALINKER UV-crosslinker (Stratagene). Microarrays are washed at room temperature once in 0.2% SDS and three times in distilled water. Non-specific binding sites are blocked by incubation of microarrays in 0.2% casein in phosphate buffered saline (PBS) (Tropix, Inc., Bedford Mass.) for 30 minutes at 60° C. followed by washes in 0.2% SDS and distilled water as before.

[0328] Hybridization

[0329] Hybridization reactions contain 9 μl of sample mixture consisting of 0.2 μg each of Cy3 and Cy5 labeled cDNA synthesis products in 5×SSC, 0.2% SDS hybridization buffer. The sample mixture is heated to 65° C. for 5 minutes and is aliquoted onto the microarray surface and covered with an 1.8 cm² coverslip. The arrays are transferred to a waterproof chamber having a cavity just slightly larger than a microscope slide. The chamber is kept at 100% humidity internally by the addition of 140 μl of 5×SSC in a corner of the chamber. The chamber containing the arrays is incubated for about 6.5 hours at 60° C. The arrays are washed for 10 min at 45° C. in a first wash buffer (1×SSC, 0.1% SDS), three times for 10 minutes each at 45° C. in a second wash buffer (0.1×SSC), and dried.

[0330] Detection

[0331] Reporter-labeled hybridization complexes are detected with a microscope equipped with an Innova 70 mixed gas 10 W laser (Coherent, Inc., Santa Clara Calif.) capable of generating spectral lines at 488 nm for excitation of Cy3 and at 632 nm for excitation of Cy5. The excitation laser light is focused on the array using a 20× microscope objective (Nikon, Inc., Melville N.Y.). The slide containing the array is placed on a computer-controlled X-Y stage on the microscope and raster-scanned past the objective. The 1.8 cm×1.8 cm array used in the present example is scanned with a resolution of 20 micrometers.

[0332] In two separate scans, a mixed gas multiline laser excites the two fluorophores sequentially. Emitted light is split, based on wavelength, into two photomultiplier tube detectors (PMT R1477, Hamamatsu Photonics Systems, Bridgewater N.J.) corresponding to the two fluorophores. Appropriate filters positioned between the array and the photomultiplier tubes are used to filter the signals. The emission maxima of the fluorophores used are 565 nm for Cy3 and 650 mn for Cy5. Each array is typically scanned twice, one scan per fluorophore using the appropriate filters at the laser source, although the apparatus is capable of recording the spectra from both fluorophores simultaneously.

[0333] The sensitivity of the scans is typically calibrated using the signal intensity generated by a cDNA control species added to the sample mixture at a known concentration. A specific location on the array contains a complementary DNA sequence, allowing the intensity of the signal at that location to be correlated with a weight ratio of hybridizing species of 1:100,000. When two samples from different sources (e.g., representing test and control cells), each labeled with a different fluorophore, are hybridized to a single array for the purpose of identifying genes that are differentially expressed, the calibration is done by labeling samples of the calibrating cDNA with the two fluorophores and adding identical amounts of each to the hybridization mixture.

[0334] The output of the photomultiplier tube is digitized using a 12-bit RTI-835H analog-to-digital (A/D) conversion board (Analog Devices, Inc., Norwood Mass.) installed in an IBM-compatible PC computer. The digitized data are displayed as an image where the signal intensity is mapped using a linear 20-color transformation to a pseudocolor scale ranging from blue (low signal) to red (high signal). The data is also analyzed quantitatively. Where two different fluorophores are excited and measured simultaneously, the data are first corrected for optical crosstalk (due to overlapping emission spectra) between the fluorophores using each fluorophore's emission spectrum.

[0335] A grid is superimposed over the fluorescence signal image such that the signal from each spot is centered in each element of the grid. The fluorescence signal within each element is then integrated to obtain a numerical value corresponding to the average intensity of the signal. The software used for signal analysis is the GEMTOOLS gene expression analysis program (Incyte).

[0336] XI. Complementary Polynucleotides

[0337] Sequences complementary to me RMEP-encoding sequences, or any parts thereof, are used to detect, decrease, or inhibit expression of naturally occurring RMEP. Although use of oligonucleotides comprising from about 15 to 30 base pairs is described, essentially the same procedure is used with smaller or with larger sequence fragments. Appropriate oligonucleotides are designed using OLIGO 4.06 software (National Biosciences) and the coding sequence of RMEP. To inhibit transcription, a complementary oligonucleotide is designed from the most unique 5′ sequence and used to prevent promoter binding to the coding sequence. To inhibit translation, a complementary oligonucleotide is designed to prevent ribosomal binding to the RMEP-encoding transcript.

[0338] XII. Expression of RMEP

[0339] Expression and purification of RMEP is achieved using bacterial or virus-based expression systems. For expression of RMEP in bacteria, cDNA is subcloned into an appropriate vector containing an antibiotic resistance gene and an inducible promoter that directs high levels of cDNA transcription. Examples of such promoters include, but are not limited to, the trp-lac (tac) hybrid promoter and the T5 or T7 bacteriophage promoter in conjunction with the lac operator regulatory element. Recombinant vectors are transformed into suitable bacterial hosts, e.g., BL21(DE3). Antibiotic resistant bacteria express RMEP upon induction with isopropyl beta-D-thiogalactopyranoside (IPTG). Expression of RMEP in eukaryotic cells is achieved by infecting insect or mammalian cell lines with recombinant Autographica californica nuclear polyhedrosis virus (AcMNPV), commonly known as baculovirus. The nonessential polyhedrin gene of baculovirus is replaced with cDNA encoding RMEP by either homologous recombination or bacterial-mediated transposition involving transfer plasmid intermediates. Viral infectivity is maintained and the strong polyhedrin promoter drives high levels of cDNA transcription. Recombinant baculovirus is used to infect Spodoptera frugiperda (Sf9) insect cells in most cases, or human hepatocytes, in some cases. Infection of the latter requires additional genetic modifications to baculovirus. (See Engelhard, E. K. et al. (1994) Proc. Natl. Acad. Sci. USA 91:3224-3227; Sandig, V. et al. (1996) Hum Gene Ther. 7:1937-1945.)

[0340] In most expression systems, RMEP is synthesized as a fusion protein with, e.g., glutathione S-transferase (GST) or a peptide epitope tag, such as FLAG or 6-His, permitting rapid, single-step, affinity-based purification of recombinant fusion protein from crude cell lysates. GST, a 26-kilodalton enzyme from Schistosoma japonicum, enables the purification of fusion proteins on immobilized glutathione under conditions that maintain protein activity and antigenicity (Amersham Pharmacia Biotech). Following purification, the GST moiety can be proteolytically cleaved from RMEP at specifically engineered sites. FLAG, ant 8-amino acid peptide, enables immunoaffinty purification using commercially available monoclonal and polyclonal anti-FLAG antibodies (Eastman Kodak). 6-His, a stretch of six consecutive histidine residues, enables purification on metal-chelate resins (QIAGEN). Methods for protein expression and purification are discussed in Ausubel (1995, supra, ch. 10 and 16). Purified RMEP obtained by these methods can be used directly in the assays shown in Examples XVI and XVII where applicable.

[0341] XIII. Functional Assays

[0342] RMEP function is assessed by expressing the sequences encoding RMEP at physiologically elevated levels in mammalian cell culture systems. cDNA is subcloned into a mammalian expression vector containing a strong promoter that drives high levels of cDNA expression. Vectors of choice include PCMV SPORT (Life Technologies) and PCR3.1 (Invitrogen, Carlsbad Calif.), both of which contain the cytomegalovirus promoter. 5-10 μg of recombinant vector are transiently transfected into a human cell line, for example, an endothelial or hematopoietic cell line, using either liposome formulations or electroporation. 1-2 μg of an additional plasmid containing sequences encoding a marker protein are co-transfected. Expression of a marker protein provides a means to distinguish transfected cells from nontransfected cells and is a reliable predictor of cDNA expression from the recombinant vector. Marker proteins of choice include, e.g., Green Fluorescent Protein (GFP; Clontech), CD64, or a CD64-GFP fusion protein. Flow cytometry (FCM), an automated, laser optics-based technique, is used to identify transfected cells expressing GFP or CD64-GFP and to evaluate the apoptotic state of the cells and other cellular properties. FCM detects and quantifies the uptake of fluorescent molecules that diagnose events preceding or coincident with cell death. These events include changes in nuclear DNA content as measured by staining of DNA with propidium iodide; changes in cell size and granularity as measured by forward light scatter and 90 degree side light scatter; down-regulation of DNA synthesis as measured by decrease in bromodeoxyuridine uptake; alterations in expression of cell surface and intracellular proteins as measured by reactivity with specific antibodies; and alterations in plasma membrane composition as measured by the binding of fluorescein-conjugated Annexin V protein to the cell surface. Methods in flow cytometry are discussed in Ormerod, M. G. (1994) Flow Cytometry, Oxford, New York N.Y.

[0343] The influence of RMEP on gene expression can be assessed using highly purified populations of cells transfected with sequences encoding RMEP and either CD64 or CD64 GFP. CD64 and CD64-GFP are expressed on the surface of transfected cells and bind to conserved regions of human immunoglobulin G (IgG). Transfected cells are efficiently separated from nontransfected cells using magnetic beads coated with either human IgG or antibody against CD64 (DYNAL, Lake Success N.Y.). mRNA can be purified from the cells using methods well known by those of skill in the art. Expression of mRNA encoding RMEP and other genes of interest can be analyzed by northern analysis or microarray techniques.

[0344] XIV. Production of RMEP Specific Antibodies

[0345] RMEP substantially purified using polyacrylamide gel electrophoresis (PAGE; see, e.g., Harrington, M. G. (1990) Methods Enzymol. 182:488-495), or other purification techniques, is used to immunize rabbits and to produce antibodies using standard protocols.

[0346] Alternatively, the RMEP amino acid sequence is analyzed using LASERGENE software (DNASTAR) to determine regions of high immunogenicity, and a corresponding oligopeptide is synthesized and used to raise antibodies by means known to those of skill in the art. Methods for selection of appropriate epitopes, such as those near the C-terminus or in hydrophilic regions are well described in the art. (See, e.g., Ausubel, 1995, supra, ch. 11.)

[0347] Typically, oligopeptides of about 15 residues in length are synthesized using an ABI 431A peptide synthesizer (Applied Biosystems) using FMOC chemistry and coupled to KLH (Sigma-Aldrich, St. Louis Mo.) by reaction with N-maleimidobenzoyl-N-hydroxysuccinimide ester (MBS) to increase immunogenicity. (See, e.g., Ausubel, 1995, supra.) Rabbits are immunized with the oligopeptide-KLH complex in complete Freund's adjuvant. Resulting antisera are tested for antipeptide and anti-RMEP activity by, for example, binding the peptide or RMEP to a substrate, blocking with 1% BSA, reacting with rabbit antisera, washing, and reacting with radio-iodinated goat anti-rabbit IgG.

[0348] XV. Purification of Naturally Occurring RMEP Using Specific Antibodies

[0349] Naturally occurring or recombinant LMEP is substantially purified by immunoaffinty chromatography using antibodies specific for RMEP. An immunoaffinity column is constructed by covalently coupling anti-RMEP antibody to an activated chromatographic resin, such as CNBr-activated SEPHAROSE (Amersham Pharmacia Biotech). After the coupling, the resin is blocked and washed according to the manufacturer's instructions.

[0350] Media containing RMEP are passed over the immunoaffinity column, and the column is washed under conditions that allow the preferential absorbance of RMEP (e.g., high ionic strength buffers in the presence of detergent). The column is eluted under conditions that disrupt antibody/RMEP binding (e.g., a buffer of pH 2 to pH 3, or a high concentration of a chaotrope, such as urea or thiocyanate ion), and RMEP is collected.

[0351] XVI. Identification of Molecules which Interact with RMEP

[0352] RMEP, or biologically active fragments thereof, are labeled with ¹²⁵I Bolton-Hunter reagent. (See, e.g., Bolton A. E. and W. M. Hunter (1973) Biochem. J. 133:529-539.) Candidate molecules previously arrayed in the wells of a multi-well plate are incubated with the labeled RMEP, washed, and any wells with labeled RMEP complex are assayed. Data obtained using different concentrations of RMEP are used to calculate values for the number, affinity, and association of RMEP with the candidate molecules.

[0353] Alternatively, molecules interacting with RMEP are analyzed using the yeast two-hybrid system as described in Fields, S. and O. Song (1989) Nature 340:245-246, or using commercially available kits based on the two-hybrid system, such as the MATCHMAKER system (Clontech).

[0354] RMEP may also be used in the PATHCALLING process (CuraGen Corp., New Haven Conn.) which employs the yeast two-hybrid system in a high-throughput manner to determine all interactions between the proteins encoded by two large libraries of genes (Nandabalan, K et al. (2000) U.S. Pat. No. 6,057,101).

[0355] XVII. Demonstration of RMEP Activity

[0356] RMEP activity is demonstrated by a polyacrylamide gel mobility-shift assay. In preparation for this assay, RMEP is expressed by transforming a mammalian cell line such as COS7, HeLa or CHO with a eukaryotic expression vector containing RMEP cDNA. The cells are incubated for 48-72 hours after transformation under conditions appropriate for the cell line to allow expression and accumulation of RMEP. Extracts containing solubilized proteins can be prepared from cells expressing RMEP by methods well known in the art. Portions of the extract containing RMEP are added to [³²P]-labeled RNA. Radioactive RNA can be synthesized in vitro by techniques well known in the art. The mixtures are incubated at 25° C. in the presence of RNase inhibitors under buffered conditions for 5-10 minutes. After incubation, the samples are analyzed by polyacrylamide gel electrophoresis followed by autoradiography. The presence of a band on the autoradiogram indicates the formation of a complex between RMEP and the radioactive transcript A band of similar mobility will not be present in samples prepared using control extracts prepared from untransformed cells.

[0357] In the alternative, ribosomal protein function of RMEP is assessed by expressing the sequences encoding ribosomal proteins at physiologically elevated levels in mammalian cell culture systems. cDNA is subcloned into a mammalian expression vector containing a strong promoter that drives high levels of cDNA expression. Vectors of choice include PCMV SPORT (Life Technologies) and PCR3.1 (Invitrogen Corporation), both of which contain the cytomegalovirus promoter (P_(CMV)) Between 5-10 μg of recombinant vector are transfected into a human cell line, preferably of endothelial or hematopoietic origin, using either liposome formulations or electroporation. 1-2 μg of an additional plasmid containing sequences encoding a marker protein are cotransfected.

[0358] Transient expression of a marker protein provides a means to distinguish transfected cells from nontransfected cells and is a reliable predictor of cDNA expression from the recombinant vector. Marker proteins of choice include, e.g., Green fluorescent Protein (GFP; Clontech), CD64, or a CD64-GFP fusion protein. Flow cytometry (FCM), an automated laser optics-based technique, is used to identify transfected cells expressing GFP or CD64-GFP and to evaluate the apoptotic state of the cells and other cellular properties.

[0359] FCM detects and quantifies the uptake of fluorescent molecules that diagnose events preceding or coincident with cell death. These events include changes in nuclear DNA content as measured by staining of DNA with propidium iodide; changes in cell size and granularity as measured by forward light scatter and 90 degree side light scatter; down-regulation of DNA synthesis as measured by decrease in bromodeoxyuridine uptake; alterations in expression of cell surface and intracellular proteins as measured by reactivity with specific antibodies; and alterations in plasma membrane composition as measured by the binding of fluorescein-conjugated Annexin V protein to the cell surface. Methods in flow cytometry are discussed in Ormerod MG (1994) Flow Cytometry, Oxford University Press, New York N.Y.

[0360] The influence of ribosomal proteins on gene expression can be assessed using highly purified populations of cells transfected with sequences encoding a ribosomal protein and either CD64 or CD64-GFP. CD64 and CD64-GFP are expressed on the surface of transfected cells and bind to conserved regions of human immunoglobulin G (IgG). Transfected cells are efficiently separated from nontransfected cells using magnetic beads coated with either human IgG or antibody against CD64 (DYNAL, Inc., Lake Success N.Y.). mRNA can be purified from the cells using methods well known by those of skill in the art. Expression of mRNA encoding a ribosomal protein and other genes of interest can be analyzed by northern analysis or microarray techniques.

[0361] In the alternative, RMEP activity is measured as the aminoacylation of a substrate tRNA in the presence of [¹⁴C]cysteine. RMEP is incubated with tRNA^(cys) and [¹⁴C]cysteine (or appropriate tRNA and amino acid substrates) in a buffered solution. [¹⁴C]-labeled product is separated from free [¹⁴C]-amino acid by chromatography, and the incorporated [¹⁴C] is quantified by scintillation counter. The amount of [¹⁴C]detected is proportional to the activity of RMEP in this assay.

[0362] In the alternative, RMEP activity is measured by incubating a sample containing RMEP in a solution containing 1 mM ATP, 5 mM Hepes-KOH (pH 7.0), 2.5 mM KCl, 1.5 mM magnesium chloride, and 0.5 mM DTT along with misacylated [¹⁴C]-Glu-tRNAGln (e.g., 1 μM) and a similar concentration of unlabeled L-glutamine. Following the quenching of the reaction with 3 M sodium acetate (pH 5.0), the mixture is extracted with an equal volume of water-saturated phenol, and the aqueous and organic phases are separated by centrifugation at 15,000×g at room temperature for 1 min. The aqueous phase is removed and precipitated with 3 volumes of ethanol at −70° C. for 15 min. The precipitated aminoacyl-tRNAs are recovered by centrifugation at 15,000×g at 4° C. for 15 min. The pellet is resuspended in of 25 mM KOH, deacylated at 65° C. for 10 min., neutralized with 0.1 M HCl (to final pH 6-7), and dried under vacuum. The dried pellet is resuspended in water and spotted onto a cellulose TLC plate. The plate is developed in either isopropanol/formic acid/water or ammonia/water/chloroform/methanol, The image is subjected to densitometric analysis and the relative amounts of Glu and Gln are calculated based on the Rf values and relative intensities of the spots. RMEP activity is calculated based on the amount of Gln resulting from the transformation of Glu while acylated as Glu-tRNA^(Gln) (adapted from Curnow, A. W. et al. (1997) Proc. Natl. Acad. Sci. 94:11819-26).

[0363] Various modifications and variations of the described methods and systems of the invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention Although the invention has been described in connection with certain embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the described modes for carrying out the invention which are obvious to those skilled in molecular biology or related fields are intended to be within the scope of the following claims. TABLE 1 Poly- Polypeptide Incyte nucleotide Incyte Incyte SEQ ID Polypeptide SEQ ID Polynucleotide Project ID NO: ID NO: ID 1622129 1 1622129CD1 48 1622129CB1 1820078 2 1820078CD1 49 1820078CB1 1527017 3 1527017CD1 50 1527017CB1 1647264 4 1647264CD1 51 1647264CB1 1721989 5 1721989CD1 52 1721989CB1 1730581 6 1730581CD1 53 1730581CB1 1740714 7 1740714CD1 54 1740714CB1 1850596 8 1850596CD1 55 1850596CB1 1856109 9 1856109CD1 56 1856109CB1 1921719 10 1921719CD1 57 1921719CB1 2099829 11 2099829CD1 58 2099829CB1 2416915 12 2416915CD1 59 2416915CB1 2472784 13 2472784CD1 60 2472784CB1 2598981 14 2598981CD1 61 2598981CB1 2738075 15 2738075CD1 62 2738075CB1 2279049 16 2279049CD1 63 2279049CB1 2660904 17 2660904CD1 64 2660904CB1 3179424 18 3179424CD1 65 3179424CB1 2885096 19 2885096CD1 66 2885096CB1 2901076 20 2901076CD1 67 2901076CB1 3074572 21 3074572CD1 68 3074572CB1 1437895 22 1437895CD1 69 1437895CB1 1454656 23 1454656CD1 70 1454656CB1  121130 24  121130CD1 71  121130CB1 1257715 25 1257715CD1 72 1257715CB1 1342022 26 1342022CD1 73 1342022CB1  194704 27  194704CD1 74  194704CB1  607270 28  607270CD1 75  607270CB1  758546 29  758546CD1 76  758546CB1  866043 30  866043CD1 77  866043CB1  927065 31  927065CD1 78  927065CB1  938071 32  938071CD1 79  938071CB1 3295984 33 3295984CD1 80 3295984CB1 4545237 34 4545237CD1 81 4545237CB1 4942964 35 4942964CD1 82 4942964CB1 5702144 36 5702144CD1 83 5702144CB1 5862945 37 5862945CD1 84 5862945CB1 6319547 38 6319547CD1 85 6319547CB1  000124 39  000124CD1 86  000124CB1 1659474 40 1659474CD1 87 1659474CB1 2267892 41 2267892CD1 88 2267892CB1 2670307 42 2670307CD1 89 2670307CB1 4524210 43 4524210CD1 90 4524210CB1 5584860 44 5584860CD1 91 5584860CB1 5807892 45 5807892CD1 92 5807892CB1 3210044 46 3210044CD1 93 3210044CB1 4942454 47 4942454CD1 94 4942454CB1

[0364] TABLE 2 Polypeptide Incyte GenBank ID Probability SEQ ID NO: Polypeptide ID NO: Score GenBank Homolog 1 1622129CD1 g8927590 1.00E−136 [fl][Homo sapiens] (AF281133) exosome component Rrp41 3 1527017CD1 g4689132 8.20E−87 30S ribosomal protein S7 homolog [Homo sapiens] 4 1647264CD1 g6651037 2.80E−38 similar to RNA binding protein [Mus musculus domesticus] 5 1721989CD1 g868267 9.80E−20 Weak similarity to ribosomal protein L14 (SP: RL14_CHLTR, P28533) [Caenorhabditis elegans]. Wilson, R. et al. (1994) 2.2 Mb of contiguous nucleotide sequence from chromosome III of C. elegans, Nature 368: 32-38. 6 1730581CD1 g3721940 7.70E−91 NO27 [Xenopus laevis] 7 1740714CD1 g2570925 6.00E−139 Survival of motor neuron protein interacting protein 1; STP1; SMN protein interacting protein 1 [Homo sapiens]. Fischer, U. et al. (1997) The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis, Cell 90: 1023-1029. 8 1850596CD1 g619302 2.80E−129 RNA-binding protein = Merc {alternatively spliced}, murine teratocarcinoma cell line, PCC4. Duhl, D. M. et al. (1994) Pleiotropic effects of the mouse lethal yellow (Ay) mutation explained by deletion of a maternally expressed gene and the simultaneous production of agouti fusion RNAs, Development 120: 1695-1708. 9 1856109CD1 g2688625 4.70E−05 Ribonuclease III (rnc) [Borrelia burgdorferi]. Fraser, C. M. et al. (1997) Genomic sequence of a Lyme disease spirochete, Borrelia burgdorferi, Nature 390: 580-586. 10 1921719CD1 g1842111 1.00E−10 decoy [Arabidopsis thaliana] 11 2099829CD1 g6015629 6.20E−89 muscle protein 684 [Mus musculus] 12 2416915CD1 g8347090 1.00E−131 [fl][Mus musculus] putative zinc finger protein FLIZ1 13 2472784CD1 g2098575 8.60E−163 F25451_2 [Homo sapiens] 14 2598981CD1 g4220489 2.80E−141 putative cleavage and polyadenylation specifity factor [Arabidopsis thaliana] ( Lin, X. et al. (1999) Nature 402: 761-768) 15 2738075CD1 g5531845 1.00E−12 [Homo sapiens] RNA-binding protein 18 3179424CD1 g7106069 8.00E−08 [fl][Schizosaccharomyces pombe] putative mitochondrial ribosomal protein; L34 family 19 2885096CD1 g5102832 3.50E−79 bK150C2.3 (PUTATIVE novel protein similar to APOBEC1 (Apolipoprotein B mRNA editing protein) and Phorbolin) [Homo sapiens] 20 2901076CD1 g7158880 0 [fl][Rattus norvegicus] serine-arginine-rich splicing regulatory protein SRRP86 21 3074572CD1 g1381029 0 RNA polymerase I associated factor (PAF53) [Mus musculus] (Hanada, K. et al. (1996) EMBO J. 15: 2217-2226) 22 1437895CD1 g2696613 6.60E−140 ATP-dependent RNA helicase #46 [Homo sapiens] 23 1454656CD1 g4981903 5.30E−09 ribosomal protein S15 [Thermotoga maritima] 24  121130CD1 g3721940 8.50E−92 NO27 [Xenopus laevis] 25 1257715CD1 g1870014 1.60E−26 pth [Mycobacterium tuberculosis] 26 1342022CD1 g304525 1.60E−76 ribosomal protein S14 [Cricetulus griseus] 27  194704CD1 g1699023 1.90E−46 putative arginine-aspartate-rich RNA binding protein [Arabidopsis thaliana] 28  607270CD1 g4138828 1.60E−18 [Candida albicans] ribosomal protein S9 small subunit precursor 29  758546CD1 g2440181 4.00E−46 putative 40s ribosomal protein [Schizosaccharomyces pombe] 30  866043CD1 g3283220 8.60E−33 splicing factor hPRP17 [Homo sapiens] 31  927065CD1 g4100563 2.60E−58 ribonuclease P protein subunit p14 [Homo sapiens] 32  938071CD1 g12654241 1.00E−102 [Homo sapiens] (BC000940) Similar to splicing factor, arginine/serine-rich 4 (SRp75) 33 3295984CD1 g673454 0 Spermatid perinuclear RNA binding protein [Mus musculus] Schumacher, J. M. et al. (1995) J. Cell Biol. 129: 1023-1032 34 4545237CD1 g6899218 1.60E−16 ribosomal protein S5 [Ureaplasma urealyticum] 35 4942964CD1 g10803047 1.00E−68 [fl][Zea mays] 40S ribosomal protein S24 36 5702144CD1 g3328106 1.10E−82 Translational release factor 1 [Homo sapiens] Zhang, Y. and Spremulli, L. L. (1998) Biochim. Biophys. Acta 1443: 245-250 37 5862945CD1 g1001933 1.30E−08 ribosomal protein L22 [Thermus thermophilus] 38 6319547CD1 g8573021 1.00E−07 [5′ incom][Leishmania major] PolyA Binding Protein 1 39  000124CD1 g3860586 1.10E−43 POLY(A) POLYMERASE (pcnB) [Rickettsia prowazekii] 40 1659474CD1 g2950473 6.70E−13 DNA-dependent rna polymerase polypeptide [Schizosaccharomyces] 41 2267892CD1 g3646126 5.70E−205 ATP-dependent RNA helicase [Homo sapiens] 42 2670307CD1 g3152934 6.20E−176 [Mus musculus] Jun coactivator Jab1 Aravind, L. and Ponting, C. P. (1998) Protein Sci. 7: 1250-1254 43 4524210CD1 g3258435 1.80E−38 389aa long hypothetical nucleolar protein [Pyrococcus] 44 5584860CD1 g3879784 1.50E−116 Similar to RNA recognition motif(aka RRM, RBD) [C. elegans] 45 5807892CD1 g1573164 5.70E−15 ribosomal protein S16 (rpS16) [Haemophilus influenzae] 46 3210044CD1 g7226601 1.30E−37 Glu-tRNA(Gln) amidotransferase, subunit A [Neisseria meningitidis]. Tettelin, H. et al. (2000) Science 287: 1809-1815. 47 4942454CD1 g790508 5.40E−51 60S acidic ribosomal protein [Zea mays]. Goddemeier, M. L. et al. (1996) Plant. Mol. Biol. 30: 655-658.

[0365] TABLE 3 Incyte Amino Potential Potential Analytical SEQ Polypeptide Acid Phosphorylation Glycosylation Signature Sequences, Methods and ID NO: ID Residues Sites Sites Domains and Motifs Databases 1 1622129CD1 245 S82, S119, Amino acid tRNA ligase motif MOTIFS S174, T226 (Aa_Trna_Ligase_Ii_1gcg_motif): Y12-D36 3′ exoribonuclease family HMMER_PFAM (RNase_PH): R13-A220 Ribonuclease PH BLIMPS_BLOCKS proteins: BL01277C: P117-L147 NUCLEOTIDYLTRANSFERASE TRANSFERASE BLAST_PRODOM POLYRIBONUCLEOTIDE PROTEIN PHOSPHORYLASE POLYNUCLEOTIDE RIBONUCLEASE PH PNPASE RNABINDING: PD002075: R13-L228 NUCLEOTIDYLTRANSFERASE; BLAST_DOMO POLYRIBONUCLEOTIDE; PHOSPHORYLASE; POLYNUCLEOTIDE DOMAIN: DM03520|P50849|1-615: L6-R222 2 1820078CD1 118 T20 N77 RIBONUCLEOPROTEIN HETEROGENEOUS BLAST_PRODOM NUCLEAR U SCAFFOLD ATTACHMENT FACTOR A HNRNP PROTEIN (ROU(1)): PD024707: P34-Y100 (p = 1.3e−05) 3 1527017CD1 179 S4, S5, S9, Signal cleavage: M1-A54 SPSCAN S10, S21, S67, Ribosomal protein S7p/S5: S4-W178 HMMER_PFAM S143 Ribosomal protein S7 protein; BLIMPS_BLOCKS BL00052A: I74-A120, BL00052B: K145-R171 Ribosomal protein S10 protein: BLIMPS_BLOCKS BL00361A: V107-K122 Ribosomal protein: PROFILESCAN ribosomal_s7.prf: M1-H83 RIBOSOMAL PROTEIN S7 30S rRNA- BLAST_PRODOM BINDING CHLOROPLAST 40S/MITOCHONDRION S5: PD000817: S5-W178 RIBOSOMAL PROTEIN S7: BLAST_DOMO DM00334|P29765|26-155: F31-R177 4 1647264CD1 101 S60, T26, T47 N19 Transmembrane domain HMMER (transmem_domain): L27-Y45, S64-V86 RNA binding protein homolog BLAST_PRODOM (R07E5.12): PD068568: P15-D101 5 1721989CD1 145 T97, S126, Y134 Signal cleavage (signal_cleavage): SPSCAN M1-S19 Ribosomal protein L14: A31-V145 HMMER_PFAM Ribosomal protein L14: BLIMPS_BLOCKS BL00049C: P94-K129 SIMILARITY TO RIBOSOMAL PROTEIN BLAST_PRODOM L14 RIBOSOMAL PROTEIN: PD080736: I32-V145 6 1730581CD1 249 T14, S18, S49, NO27 PROTEIN (predicted nucleolar BLAST_PRODOM S75, S133, T243 protein): PD173812: M1-L113 NUCLEOLIN: BLAST_DOMO DM02740|S32644|630-703: R141-G205 RNA-BINDING RGG-BOX DOMAIN: BLAST_DOMO DM04007|S49193|21-239: G103-R202 7 1740714CD1 265 S19, T48, S81, N83, N132 PROTEIN SURVIVAL OF MOTOR NEURON BLAST_PRODOM T112, S138, INTERACTING: S178, S227, PD039299: M25-D262 S235 8 1850596CD1 306 S2, T11, S36, N9, N261 Rnp_1 motif: K55-Y62 MOTIFS S177, S199, RNA recognition motif. (a.k.a. RRM HMMER_PFAM S206, S252, and RBD): rrm: V23-I87 T262, T275, RIBONUCLEOPROTEIN NUCLEAR PROTEIN BLAST_PRODOM T286, S288, RNABINDING HNRNP HETEROGENEOUS C1 T298, NUCLEOPROTEIN C PHOSPHORYLATION: PD015984: N88-D220 RNA; EUKARYOTIC; C2; BLAST_DOMO RIBONUCLEOPROTEIN DOMAIN: DM08081|A47318|6-293: Q6-A304 Eukaryotic RNA-binding domain: BLIMPS_BLOCKS BL00030B: K55-N64 9 1856109CD1 332 S61, S121, N82, N249, Signal peptide (signal_peptide): HMMER T161, T179, N315 M1-G30 S206, T224, Double-stranded RNA binding motif HMMER_PFAM S251, T322, (dsrm): P237-L304 (score = 0.1) HYPOTHETICAL 49.1 KD PROTEIN BLAST_PRODOM F02A9.4 IN CHROMOSOME III: PD140911: D67-R311 PROTEIN RNABINDING RNA REPEAT BLAST_PRODOM DEAMINASE HYDROLASE ADENOSINE DOUBLESTRANDED III NUCLEAR: PD001171: P237-L304 (p = 0.0090) 10 1921719CD1 279 S28, S85, T138, Signal cleavage (signal_cleavage): SPSCAN T183, T194, M1-G42 T214, T256 DECOY 60S RIBOSOMAL PROTEIN L30 BLAST_PRODOM MITOCHONDRIAL PRECURSOR YML30 MITOCHONDRION TRANSIT: PD037326: R136-P209 (p = 1.6e−08) 11 2099829CD1 239 S4, S11, T15 N106 Ribosomal protein L10 HMMER_PFAM T36, Y39, S80, (Ribosomal_L10): K18-T117 S93, T105, PROTEIN RIBOSOMAL SIMILAR 60S BLAST_PRODOM T108, T120, ACIDIC PO UFD4CAP1 INTERGENIC Y124, S171, REGION: T203, S212, PD037726: M1-G213 S225, S229, RAT ACIDIC RIBOSOMAL PROTEIN: BLAST_DOMO S233, S235, DM00904|P29764|1-318: V10-S212 12 2416915CD1 291 T18 T20 T32 T37 SUPPRESSOR OF SABLE RNA-BINDING BLAST_PRODOM S77 T113 S165 NUCLEAR HOMOLOG T235 S59 S112 PD032978: K221-K288 T285 S289 Y76 13 2472784CD1 451 S29 S131 S337 Eukaryotic putative RNA-binding MOTIFS S338 S343 S399 region RNP-1 Signature S290 T389 K393-F400 ATP/GTP-binding site motif A (P- MOTIFS loop) G22-S29 RNA recognition motif. (RRM, RBD, HMMER_PFAM or RNP domain) I354-L425 Eukaryotic RNA-binding BLAST_BLIMPS BL00030A: I354-F372 BL00030B: K393-D402 F25451_2 BLAST_PRODOM PD057917: L144-R206 PD056050: G305-R353 RIBONUCLEOPROTEIN REPEAT BLAST_DOMO DM00012|Q10355|25-106: W347-S428 DM00012|P32588|154-238: D350-L425 DM00012|P31483|87-172: A349-K424 DM00012|Q05966|1-83: D351-S428 14 2598981CD1 600 T209 T254 T520 POLYADENYLATION CLEAVAGE BLAST_PRODOM T577 S213 T272 SPECIFICITY RNA BINDING T512 Y50 Y175 PD005421: Y179-L370 15 2738075CD1 217 T207 T47 S198 N66 Eukaryotic putative RNA-binding MOTIFS T22 S155 S193 region RNP-1 T194 S210 Signature K51-F58 signal_cleavage: SPSCAN M1-A64 RNA recognition motif. (RRM, RBD, HMMER_PFAM or RNP domain) rrm: V12-A83 Eukaryotic RNA-binding region BLIMPS_BLOCKS RNP-1 proteins BL00030A: V12-F30 BL00030B: K51-D60 Eukaryotic putative RNA-binding PROFILESCAN region RNP-1 signature rnp_1.prf: N23-I85 RIBONUCLEOPROTEIN REPEAT BLIMPS_DOMO DM00012|S20940|151-238: V12-A86 DM00012|Q04836|234-321: V12-A86 DM00012|P19339|205-288: S10-N73 DM00012|P38159|3-84: P7-A86 16 2279049CD1 319 S275 T20 S234 N153 Aminoacyl-transfer RNA synthetases MOTIFS T264 S80 T119 class-II T268 Signatures H255-E278 17 2660904CD1 108 Ribosomal protein S15 signature PROFILESCAN G30-G101 18 3179424CD1 92 S71 T12 signal_cleavage: SPSCAN M1-S15 Ribosomal protein L34 HMMER_PFAM N51-H92 Ribosomal protein L34 BLIMPS_BLOCKS BL00784: G50-R87 19 2885096CD1 268 T78 T162 S241 N109 N193 Cytidine and deoxycytidylate MOTIFS Y91 T198 S222 deaminases zinc-binding region signature H144-V182 signal_cleavage: SPSCAN M1-S21 Cytidine and deoxycytidylate BLIMPS_BLOCKS deaminases zinc-binding region BL00903: Y169-C178 APOLIPOPROTEIN B MRNA EDITING BLAST_DOMO PROTEIN DM04741|P51908|1-228: K129-V239 DM04741|P41238|1-235: H144-V239 DM04741|A53853|1-236: H144-V239 20 2901076CD1 624 S329 S351 S359 N25 N254 N339 RNA recognition motif. (RRM, RBD, HMMER_PFAM S367 T380 S502 N485 N570 or RNP domain) S519 S520 S558 N616 rrm: V184-I253 S61 S297 S319 rrm: I21-V93 S324 S487 S493 ARGININE RICH SPLICEOSOME SPLICING BLAST_PRODOM S505 S508 T511 FACTOR T514 S524 S543 PD037489: V20-G139 S553 S573 S618 TYPE B REPEAT REPEAT BLAST_DOMO T159 S175 T194 DM05511|S26650|1-1203: P264-R539 S557 T619 DM05511|P18583|113-1296: P264-R539 21 3074572CD1 419 S8 S20 T64 T130 N93 N161 N237 RNA POLYMERASE I DNA DIRECTED BLAST_PRODOM T144 T153 S331 TRANSFERASE TRANSCRIPTION NUCLEAR S364 S380 S409 PROTEIN S296 S385 T419 PD025048: Q21-R415 T42 S137 T174 S221 S230 T239 S265 S390 22 1437895CD1 743 S11 S25 S70 N10 N154 N425 DEAH-box subfamily ATP-dependent BLIMPS_BLOCKS S341 S383 S561 N473 N560 helicase proteins: S671 T732 S13 N577 BL00690A: G85-Q94 S49 T325 S351 BL00690B: T116-E133 S397 T642 T658 BL00690C: I182-S191 Y247 Y293 Y602 DEAD and DEAH box families ATP- PROFILESCAN dependent helicases signatures (deah_atp_helicase.prf): D163-P209 ATP-dependent RNA helicase: BLAST_PRODOM PD001259: F401-H544 DEAH-box subfamily ATP-dependent BLAST_DOMO helicases: DM00649|P53131|84-705: L55-Y677 Atp_Gtp_A: MOTIFS G85-S92 23 1454656CD1 284 S57 S160 T232 Ribosomal protein S15 HMMER_PFAM T244 T279 S88 (Ribosomal_S15): S165 T200 S151-E215 Ribosomal protein S15 signature PROFILESCAN (ribosomal_s15.prf): P146-E215 24 121130CD1 248 T14 S49 S74 NO27 protein (PD173812): M1-L112 BLAST_PRODOM S132 S18 T242 Nucleolin: BLAST_DOMO DM02740|S32644|630-703: R140-G204 25 1257715CD1 214 S137 T112 S181 Peptidyl-tRNA hydrolase HMMER_PFAM (Pept_tRNA_hydro): W31-Q208 Peptidyl-tRNA hydrolase: BLIMPS_BLOCKS BL01195B: L88-G99 BL01195C: V116-N154 BL01195D: M156-G164 Peptidyl-tRNA hydrolase BLAST_PRODOM (PD005324): M32-I199 Peptidyl-tRNA hydrolase: BLAST_DOMO DM02080|P44682|1-193: M32-I199 26 1342022CD1 184 T2 S16 S19 S81 N71 N136 Ribosomal protein S11 HMMER_PFAM S172 T173 S69 (Ribosomal_S11): G62-R180 Ribosomal protein S11: BLIMPS_BLOCKS BL00054A: G62-S102 BL00054B: K139-R180 Ribosomal_S11: G144-L184 PROFILESCAN Ribosomal protein S11 BLAST_PRODOM (PD001010): G62-R180 E. coli ribosomal protein S11: BLAST_DOMO DM00861|P19950|16-148: G51-L184 Ribosomal_S11: D164-D171 MOTIFS 27 194704CD1 371 S270 S280 S291 Aspartate-arginine-rich mRNA BLAST_PRODOM S317 T17 S120 binding protein (PD017473): S152 S257 T283 F30-K230 S321 S339 S342 RNP-1: BLAST_DOMO S360 T52 T111 DM03434|P08621|359-483: R204-K323 T231 S332 Y173 28 607270CD1 396 S13 T63 S64 signal_peptide: M1-A25 HMMER T153 S252 T278 Ribosomal protein S9/S16 HMMER_PFAM S290 T392 T68 (Ribosomal_S9): T100 S214 S270 G274-R396 T357 Y218 Y262 Ribosomal protein S9: BLIMPS_BLOCKS BL00360A: K275-Q301 BL00360B: F317-L352 BL00360C: L370-R396 Ribosomal protein S9 signature PROFILESCAN (ribosomal_s9.prf): I306-R396 Ribosomal protein S9 (PD001627): BLAST_PRODOM G274-R396 Ribosomal protein S9: BLAST_DOMO DM00779|P38120|149-277: D263-R396 Ribosomal_S9: MOTIFS G334-L352 29 758546CD1 184 S153 T159 S163 S4 domain (S4): HMMER_PFAM Y48 R109-D156 Ribosomal protein S4: BLAST_DOMO DM00205|P32899|101-174: V101-Y173 30 866043CD1 282 T10 S67 T76 WD domain, G-beta repeat: HMMER_PFAM T103 S109 S136 WD40: G20-D58 S153 S200 S239 WD40: E60-D100 T5 T57 S131 WD40: M199-S239 WD40: A243-H282 31 927065CD1 125 T65 Y21 MOTIFS 32 938071CD1 365 S23 S24 S132 N69 MOTIFS T172 S186 S187 S201 S202 S210 S254 S261 S116 S132 T161 S176 T177 S178 S213 S215 S217 S219 S223 S224 S257 S265 S269 T282 T300 S301 S325 S350 S24 S27 S33 S36 S71 S110 S125 S149 S193 S202 S246 Y324 33 3295984CD1 672 Y137 Y297 S24 N72 N180 N472 L381-L402 Leucine_Zipper MOTIFS S36 T56 T58 N476 N482 Double-stranded RNA binding BLIMPS_PFAM T120 S182 S343 N485 N486 protein: T345 T427 T455 N489 G554-A567 S465 S470 S474 Double-stranded RNA binding motif: HMMER_PFAM S490 S496 S3 L388-M451, G511-L574 T52 T120 T159 RNA-binding Protein BLIMPS_PRODOM S182 S201 S333 L448-M464, G411-V424, N558-A567 T345 S435 T438 ZINC FINGER RNA BINDING SPERMATID BLAST_PRODOM S510 PROTEIN R80-D329 SPERMATID PERINUCLEAR RNA BINDING BLAST_PRODOM PROTEIN F575-G648, P330-L392, G452-N513 TRANSCRIPTION; RNA; SPERMATID; BLAST_DOMO PERINUCLEAR M1-P369 DOUBLE-STRANDED RNA BINDING DOMAIN BLAST_DOMO N370-I461, T494-K584 34 4545237CD1 430 S240 T94 S161 signal peptide HMMER T214 T232 S354 M1-G20 T118 T232 T262 Ribosomal protein S5 HMMER_PFAM S295 S386 I222-G352 Ribosomal protein S5 pro BLIMPS_BLOCKS T220-A271 I303-S339 Ribosomal protein S5 signature PROFILESCAN I222-R284 RIBOSOMAL PROTEIN S5 BLAST_PRODOM I222-N341 RIBOSOMAL PROTEIN S5 BLAST_DOMO R226-G367 35 4942964CD1 137 T11 T14 T19 N39 Ribosomal_S24e MOTIFS S109 Y95 S41 F70-N84 T104 F28-K111 Ribosomal protein S24e HMMER_PFAM Ribosomal protein S24e signature PROFILESCAN E47-A103 Ribosomal protein S24e BLIMPS_BLOCKS V10-E54, I61-K105 Arginine repressor BLIMPS_PFAM N20-G71 Protein S24E BLAST_DOMO V10-K146 RIBOSOMAL 40S S24 S24E BLAST_PRODOM V29-K111 36 5702144CD1 380 Y169 S247 T45 N255 N340 Leucine_Zipper MOTIFS T342 S362 S371 L57-L78 L64-L85 L71-L92 T208 T243 S321 Rf_Prok_I MOTIFS S377 R245-V261 signal peptide HMMER M1-G20 Prokaryotic-type class I peptide HMMER_PFAM chain release factor RF-1 G138-R338 Prokaryotic-type class I peptide BLIMPS_BLOCKS chain release factors signature E123-R161, I184-Q226, D238-K284, G316-R338 PROKARYOTIC-TYPE CLASS I PEPTIDE BLAST_DOMO CHAIN RELEASE FACTORS L224-S377 PEPTIDE CHAIN RELEASE FACTOR BLAST_PRODOM G138-R338 37 5862945CD1 206 S42 S141 Y83 Signal peptide SPSCAN M1-T35 Ribosomal protein L22 BLIMPS_BLOCKS H69-K105, V128-L172 Ribosomal protein L22 signature PROFILESCAN R131-E192 38 6319547CD1 190 S96 T140 S188 N12 N136 Rnp_1 MOTIFS T178 T179 S20 R69-F76 T78 S128 Eukaryotic putative RNA-binding PROFILESCAN region RNP-1 signature L45-K97 RNA recognition motif HMMER_PFAM L27-V101 Eukaryotic RNA-binding BLIMPS_BLOCKS L27-L45 R69-T78 39 000124CD1 434 S18 S47 T165 N272 N152 Poly A polymerase family HMMER_PFAM S274 T307 S389 N199 N217 T110-E276 S400 T29 T112 RNA BINDING PROCESSING BLAST_PRODOM T124 S289 T359 POLYNUCLEOTIDE Y368 G63-G248 RNA BINDING POLYMERASE BLAST_DOMO L51-G248 40 1659474CD1 339 S60 T244 S329 MOTIFS T69 T254 T315 Y238 41 2267892CD1 599 T18 T79 S86 Atp_Gtp_A MOTIFS S129 S213 S282 A209-T216 S283 S320 S344 Helicase conserved C-terminal BLIMPS_PFAM T397 S457 T503 domain T569 S589 S22 Y496-T503 T92 T585 S77 DEAD/DEAH box helicase HMMER_PFAM S99 S110 S381 Q178-E389 S492 T517 Helicases conserved C-terminal HMMER_PFAM domain K426-G507 DEAD-box subfamily ATP-dependent BLIMPS_BLOCKS helicases G184-P222, M225-I250, V312-L335, V465-G510 DEAD-BOX SUBFAMILY ATP-DEPENDENT BLAST_DOMO HELICASES N179-I542 RNA BINDING NUCLEAR DNA FACTOR BLAST_PRODOM I422-G507, D182-S258 42 2670307CD1 334 S24 S148 S231 N332 Mov34/MPN/PAD1 family HMMER_PFAM T257 T310 S270 H50-A314 S307 SUBUNIT 26S MOV34 S12 PAD1 HOMOLOG BLAST_PRODOM F52-R282 PAD1 related protein BLAST_DOMO I57-S254 43 4524210CD1 448 S159 T285 S319 Nol1_Nop2_Sun MOTIFS T355 T413 S417 F296-G307 Y182 T33 S159 NOL1/NOP2/sun family HMMER_PFAM S265 Y194-K369 NOL1/NOP2/sun family BLIMPS_BLOCKS I217-I231, G239-G262, F296-G309, K342-L367 NUCLEOLAR SUN P120 PROLIFERATING BLAST_PRODOM CELL ANTIGEN R176-E379 NOL1/NOP2/FMU FAMILY L197-V363 BLAST_DOMO 44 5584860CD1 420 S218 S86 S102 N294 RNA recognition motif HMMER_PFAM S126 S142 T187 L234-V300 T242 T244 S102 RNA-binding motif BLIMPS_BLOCKS Y181 L234-F252 RNA BINDING PROTEIN BLAST_PRODOM L223-E314 45 5807892CD1 137 T18 T27 S122 Ribosomal protein S16 HMMER_PFAM S60 T105 T125 G24-S84 T130 Ribosomal protein S16 BLIMPS_BLOCKS H16-L51, L68-A94 RIBOSOMAL S16 NUCLEASE G25-A81 BLAST_PRODOM 46 3210044CD1 556 T30, T64, N165, N199 AMIDASES: BLAST_DOMO T153, 210, DM00646|A53101|91-465: V94-G338 S231, S254, Amidase proteins: BLIMPS_BLOCKS S344, T353, BL00571: N219-S270 S389, S458 Amidase signature (amidases.prf): PROFILESCAN G235-G278 Transmembrane domain HMMER (transmem_domain): I33-P58 Amidase: HMMER_PFAM D93-P313, R443-L537 Signal cleavage: M1-G56 SPSCAN 47 4942454CD1 111 S19, S47, S101, RAT ACIDIC RIBOSOMAL PROTEIN P1: BLAST_DOMO S108 DM00632|S54179|1-112: M1-D111 Ribosomal protein P2 Signature: BLIMPS_PRINTS PR00456E: A75-A89; PR00456F: K98-L109 RIBOSOMAL PROTEIN, ACIDIC 60S BLAST_PRODOM PHOSPHORYLATION P2, P1, L12 MULTIGENE FAMILY: PD001928: M1-D111 60S acidic ribosomal protein HMMER_PFAM (60s_ribosomal): M1-D111

[0366] TABLE 4 Incyte Polynucleotide Polynucleotide Sequence Selected 5′ 3′ SEQ ID NO: ID Length Fragments Sequence Fragments Position Position 48 1622129CB1 882 1-59 642017H1 (BRSTNOT03) 1 270 483782F1 (HNT2RAT01) 176 882 49 1820078CB1 1220 1-41, 71164239V1 647 1220 833-1220 70024116D1 564 1220 1293767T6 (PGANNOT03) 403 1203 6571082H1 (MCLDTXN05) 1 490 50 1527017CB1 2020 1-209, 1541283H1 (SINTTUT01) 1266 1473 1415-2020 1824377H1 (GBLATUT01) 1 265 1659084T6 (URETTUT01) 1279 2020 1527017T1 (UCMCL5T01) 744 1407 SBMA03026F1 324 858 1438348F1 (PANCNOT08) 226 769 51 1647264CB1 637 1-40 2735749H2 (OVARNOT09) 286 508 1647264H1 (PROSTUT09) 149 384 g1136841 1 637 52 1721989CB1 717 1-21 1721989F6 (BLADNOT06) 1 419 079812F1 (SYNORAB01) 146 717 53 1730581CB1 2061 1-24, 1525770T1 (UCMCL5T01) 1109 1566 1219-1514 1457506F6 (COLNFET02) 486 1012 915914R1 (BRSTNOT04) 306 884 1730581F6 (BRSTTUT08) 1546 2061 2693987T6 (LUNGNOT23) 953 1565 102784H1 (ADRENOR01) 1 406 54 1740714CB1 1307 1-43, 1740714CT1 (HIPONON01) 1 1307 1111-1142 3074962H1 (BONEUNT01) 1 277 55 1850596CB1 1357 820443R1 (KERANOT02) 493 1131 2018418H1 (THP1NOT01) 813 1160 1989582H1 (CORPNOT02) 986 1357 1855681H1 (HNT3AZT01) 1 270 3563740H1 (SKINNOT05) 141 470 3147502H1 (PENCNOT05) 282 643 56 1856109CB1 1749 1-29, 6708693H1 (HEAADIR01) 1411 1738 1201-1749 1518037F1 (BLADTUT04) 460 979 2367008F6 (ADRENOT07) 1547 1749 875652T1 (LUNGAST01) 1073 1718 1981031R6 (LUNGTUT03) 563 1109 1806093F6 (SINTNOT13) 1 525 57 1921719CB1 991 1-79 1921719T6 (BRSTTUT01) 335 973 902176H1 (BRSTTUT03) 697 991 1522552F1 (BLADTUT04) 1 429 58 2099829CB1 1188 1024-1188 g1155846 718 1065 1868148T6 (SKINBIT01) 402 972 1984185T6 (LUNGAST01) 248 889 3135711H1 (SMCCNOT01) 1 274 59 2416915CB1 1454 1-22 313888H1 (LUNGNOT02) 690 1006 1569836F6 (UTRSNOT05) 37 519 3177069T6 (UTRSTUT04) 830 1454 2172869H1 (ENDCNOT03) 761 1026 3873555H1 (HEARNOT06) 446 741 3584701H1 (293TF4T01) 1 315 60 2472784CB1 1588 1-242, 1926194R6 (BRSTNOT02) 1161 1588 288-726 2701446H1 (OVARTUT10) 775 1135 908518R2 (COLNNOT09) 1 616 2834469H1 (TLYMNOT03) 1 274 599142R6 (BRSTNOT02) 1229 1588 2023191F6 (CONNNOT01) 1038 1588 2470222F6 (THP1NOT03) 546 1113 1727193H1 (PROSNOT14) 387 634 61 2598981CB1 2111 557-1153, 1593669X16C1 289 954 1-22 (BRAINOT14) SBZA06347V1 936 1527 SBZA04028V1 1236 2111 1593669X11C1 52 711 (BRAINOT14) SBZA02427V1 1159 1621 2450029H1 (ENDANOT01) 1 227 62 2738075CB1 1155 1-36, 222536F1 (PANCNOT01) 15 622 597-623 2055577R6 (BEPINOT01) 801 1155 222536R1 (PANCNOT01) 55 1155 63 2279049CB1 1673 1597077F6 (BRAINOT14) 445 1005 438020T6 (THYRNOT01) 938 1650 1798393F6 (COLNNOT27) 1208 1673 2458985F6 (ENDANOT01) 1 458 3050984H1 (LUNGNOT25) 409 687 64 2660904CB1 584 1-229, 71284614V1 387 584 519-584 70937372V1 1 514 65 3179424CB1 978 1-189 3204102F6 (PENCNOT03) 1 632 586088F1 (PROSNOT02) 307 978 66 2885096CB1 1055 1-278 1702519X13C1 127 778 (BLADTUT05) 3887887H1 (UTRSNOT05) 813 1055 1876565F6 (LEUKNOT03) 552 1043 2885096F6 (SINJNOT02) 1 454 67 2901076CB1 2220 1189-1491, 5635858H1 (UTRSTMR01) 1333 1585 634-662 3524308H1 (ESOGTUN01) 333 644 1285251F6 (COLNNOT16) 552 1152 3254924X309D1 39 491 (OVARTUN01) 1260590R1 (SYNORAT05) 892 1508 5117929H1 (SMCBUNT01) 1 278 1285251T1 (COLNNOT16) 792 1218 1852576F6 (LUNGFET03) 1730 2220 2921502H1 (SININOT04) 1457 1740 4936943H1 (OVARNON03) 1665 1904 68 3074572CB1 1890 1-24, 1558589F1 (SPLNNOT04) 1011 1432 1837-1890 SAEA01339F1 1325 1890 157743R6 (THP1PLB02) 221 725 SAEA01587F1 769 1343 3173159H1 (UTRSTUT04) 1 278 SAEA01593R1 286 843 69 1437895CB1 2893 845-1749, 2630813H1 (COLNTUT15) 2042 2283 1-43, 4919358H1 (TESTNOT11) 1384 1615 2872-2893 3205068H1 (PENCNOT03) 1623 1888 3877384F6 (HEARNOT06) 305 799 1493166R6 (PROSNON01) 2324 2884 4840634H1 (OSTENOT01) 903 1171 3550295H1 (BRONDIT01) 1 244 6453094H1 (COLNDIC01) 192 757 1400075F1 (BRAITUT08) 1046 1606 g1377484 2337 2893 1437895T1 (PANCNOT08) 2244 2863 786771F1 (PROSNOT05) 2707 2892 1582477H1 (DUODNOT01) 1599 1793 g1102494 2314 2892 1437895F1 (PANCNOT08) 1731 2278 3628841F6 (COLNNOT38) 722 1098 70 1454656CB1 885 1-47 782659R1 (MYOMNOT01) 523 885 938801R1 (CERVNOT01) 505 876 876916T1 (LUNGAST01) 280 867 4843096H1 (OSTENOT01) 23 314 g1617769 1 414 71 121130CB1 1269 1-42 1457506F6 (COLNFET02) 530 1055 915914R1 (BRSTNOT04) 352 929 3730083H1 (SMCCNON03) 974 1269 5217827H1 (BRSTNOT35) 258 521 5376327H1 (BRAXNOT01) 14 254 g1716816 1 395 102784H1 (ADRENOR01) 63 452 72 1257715CB1 1066 835-1066, g3048792 746 1066 1-22 1680736H1 (STOMFET01) 1 221 1901049F6 (BLADTUT06) 320 825 1731204F6 (BRSTTUT08) 17 669 73 1342022CB1 639 1-98 1908142T6 (CONNTUT01) 1 614 2257149R6 (OVARTUT01) 100 639 74 194704CB1 1420 822-852, 834691H1 (PROSNOT07) 1181 1420 1051-1420 1701714F6 (BLADTUT05) 32 698 1822010F6 (GBLATUT01) 361 983 2584972H1 (BRAITUT22) 1156 1420 1395146H1 (THYRNOT03) 1 255 2060393R6 (OVARNOT03) 807 1420 75 607270CB1 1457 1-103, 607270H1 (BRSTTUT01) 1 265 680-892 607270X11 (BRSTTUT01) 104 745 1558989F6 (SPLNNOT04) 448 973 449792F1 (TLYMNOT02) 780 1457 76 758546CB1 1184 1-53 1488271H1 (UCMCL5T01) 429 691 489544F1 (HNT2AGT01) 506 1184 489544R1 (HNT2AGT01) 58 664 2657989H1 (LUNGTUT09) 1 229 77 866043CB1 1638 1-561 5278386H1 (MUSLNOT01) 693 891 004388T6 (HMC1NOT01) 990 1615 5039960H1 (COLHTUT01) 704 952 866043R6 (BRAITUT03) 1266 1638 2295207R6 (BRSTNOT05) 171 638 3398785H1 (UTRSNOT16) 1 226 5421565H1 (PROSTMT07) 468 715 004388R6 (HMC1NOT01) 838 1355 78 927065CB1 701 SXAF04722V1 254 701 SXAE03477V1 13 411 g1545603 1 614 79 938071CB1 1829 1070-1829, 2570862T6 (HIPOAZT01) 852 1407 513-561, 2344188T6 (TESTTUT02) 168 744 828-910, 2061053R6 (OVARNOT03) 1077 1413 689-768 2962659T6 (ADRENOT09) 296 882 2371642H1 (ADRENOT07) 1210 1425 g1141976 1335 1829 3148824H1 (ADRENON04) 1 274 80 3295984CB1 2541 1-242, SCGA02064V1 287 1013 2385-2541 SCGA02183V1 1784 2326 261729R6 (HNT2AGT01) 1055 1668 SCGA00610V1 1221 1778 SCGA10196V1 1588 2118 4526287F6 (LYMBTXT01) 1 532 3813241H1 (TONSNOT03) 2255 2541 SCGA05805V1 591 1162 81 4545237CB1 1647 525-567 1561512F6 (SPLNNOT04) 219 830 1639525F6 (UTRSNOT06) 1226 1647 1649445F6 (PROSTUT09) 874 1378 2013721X28C1 560 1154 (TESTNOT03) 5882142H1 (LIVRNON08) 559 832 567202H1 (MMLR3DT01) 1 252 82 4942964CB1 735 704-735 4942964T6 (BRAIFEN05) 1 735 83 5702144CB1 2614 1-93, 1481581F6 (CORPNOT02) 724 1378 1719-1901 2287840X12F1 464 906 (BRAINON01) 1962628R6 (BRSTNOT04) 2107 2614 2160148F6 (ENDCNOT02) 1866 2324 2287840X14F1 370 861 (BRAINON01) 1329248F1 (PANCNOT07) 1529 2094 968129X11F1 1093 1612 (BRSTNOT05) 1635830F6 (UTRSNOT06) 1 454 84 5862945CB1 736 1-34 280637F1 (LIVRNOT02) 106 736 2244058F6 (PANCTUT02) 1 510 85 6319547CB1 1046 1-33 2383076F6 (ISLTNOT01) 574 1046 3014264H1 (MUSCNOT07) 509 809 5571304F6 (TLYMNOT08) 142 782 591563H1 (BRAVUNT02) 1 241 86 000124CB1 2266 1-32, 000124T6 (U937NOT01) 1742 2266 2085-2266 789548R6 (PROSTUT03) 1100 1600 3519565R6 (LUNGNON03) 1196 1782 902790R6 (BRSTTUT03) 629 1123 3039556F6 (BRSTNOT16) 1 611 SBZA03954V1 482 1008 87 1659474CB1 1041 927-954, 1865044F6 (PROSNOT19) 615 1041 677-709, SAYA00579F1 352 833 833-857 4005010F6 (ENDCNOT04) 1 533 88 2267892CB1 2722 2347-2722 2290718X14F1 726 1230 (BRAINON01) 3139431F6 (SMCCNOT02) 529 1043 1970333F6 (UCMCL5T01) 888 1350 3815067H1 (TONSNOT03) 1574 1844 082326R1 (HUVESTB01) 1828 2448 082326F1 (HUVESTB01) 2007 2710 2287150X13F1 1 546 (BRAINON01) 256073F1 (HNT2RAT01) 2581 2722 3925865H1 (KIDNNOT19) 1219 1479 1420665F1 (KIDNNOT09) 1276 1828 89 2670307CB1 1287 1-382 008243F1 (HMC1NOT01) 315 1287 1295856F1 (PGANNOT03) 969 1287 1304866F1 (PLACNOT02) 732 1287 1353856F1 (LATRTUT02) 1 485 90 4524210CB1 2226 509-1516 SCIA00216V1 430 1034 SCIA00181V1 1251 1780 2256793X309B2 1645 2225 (OVARTUT01) SCIA03684V1 1161 1705 2256793X318D4 1 517 (OVARTUT01) 2058779H1 (OVARNOT03) 1999 2226 SCIA02060V1 665 1237 91 5584860CB1 2362 1-49, 1965766R6 (BRSTNOT04) 1954 2362 1066-2362 1850306T6 (LUNGFET03) 1698 2340 842676R1 (PROSTUT05) 712 1279 71054273V1 (SG0000314) 1 614 2105411R6 (BRAITUT03) 1293 1767 SAEB02217F1 1191 1752 377688R6 (NEUTFMT01) 541 1153 92 5807892CB1 731 1-68 3745266F6 (THYMNOT08) 1 495 958760R1 (KIDNNOT05) 416 731 93 3210044CB1 2088 2051-2088, 70822015V1 557 1148 1-190, 7705613J1 (UTRETUE01) 1 541 648-1486, 70821405V1 1195 1807 1811-1843 70818955V1 511 1069 6016193H1 (HNT2UNN03) 1127 1739 70821946V1 (SG0000294) 1653 2088 94 4942454CB1 660 1-23 4942454T6 (BRAIFEN03) 3 660 4942454F6 (BRAIFEN03) 1 589

[0367] TABLE 5 Polynucleotide SEQ ID NO: Incyte Project ID Representative Library 48 1622129CB1 HNT2RAT01 49 1820078CB1 LUNGNOT20 50 1527017CB1 LUNGNOT14 51 1647264CB1 LUNGNOT27 52 1721989CB1 ISLTNOT01 53 1730581CB1 LUNGTUT03 54 1740714CB1 TLYMNOT02 56 1856109CB1 BLADTUT04 57 1921719CB1 BRSTTUT01 58 2099829CB1 ENDANOT01 59 2416915CB1 BLADTUT05 60 2472784CB1 BRSTNOT02 61 2598981CB1 LIVRNON08 62 2738075CB1 BRAITUT02 63 2279049CB1 BRAINOT14 64 2660904CB1 LUNGTUT09 65 3179424CB1 KIDNNOT09 66 2885096CB1 BLADTUT04 67 2901076CB1 ENDCNON02 68 3074572CB1 SINTFET03 69 1437895CB1 PANCNOT08 70 1454656CB1 ADRENOT03 71  121130CB1 SPLNFET01 72 1257715CB1 MENITUT03 73 1342022CB1 COLNFET02 74  194704CB1 OVARNOT03 76  758546CB1 COLNNOT11 77  866043CB1 BRAITUT03 78  927065CB1 LNODNOT03 79  938071CB1 EPIPNON05 80 3295984CB1 THP1NOT03 81 4545237CB1 SPLNNOT04 82 4942964CB1 BRAIFEN05 83 5702144CB1 PANCNOT07 84 5862945CB1 KERANOT01 85 6319547CB1 PROSNOT16 86  000124CB1 KIDNNOT05 87 1659474CB1 KERANOT01 88 2267892CB1 UCMCL5T01 89 2670307CB1 BRSTTUT01 90 4524210CB1 OVARTUT01 91 5584860CB1 UTRSNOT05 92 5807892CB1 KIDNTUT01 93 3210044CB1 PITUNOT01 94 4942454CB1 BRAIFEN03

[0368] TABLE 6 Library Vector Library Description ADRENOT03 PSPORT1 Library was constructed using RNA isolated from the adrenal tissue of a 17-year-old Caucasian male, who died from cerebral anoxia. BLADTUT04 pINCY Library was constructed using RNA isolated from bladder tumor tissue removed from a 60-year-old Caucasian male during a radical cystectomy, prostatectomy, and vasectomy. Pathology indicated grade 3 transitional cell carcinoma in the left bladder wall. Carcinoma in-situ was identified in the dome and trigone. Patient history included tobacco use. Family history included type I diabetes, malignant neoplasm of the stomach, atherosclerotic coronary artery disease, and acute myocardial infarction. BLADTUT05 pINCY Library was constructed using RNA isolated from bladder tumor tissue removed from a 66-year-old Caucasian male during a radical prostatectomy, radical cystectomy, and urinary diversion. Pathology indicated grade 3 transitional cell carcinoma on the anterior wall of the bladder. Patient history included lung neoplasm and tobacco abuse in remission. Family history included malignant breast neoplasm, tuberculosis, cerebrovascular disease, atherosclerotic coronary artery disease, and lung cancer. BRAIFEN03 pINCY This normalized fetal brain tissue library was constructed from 3.26 million independent clones from a fetal brain library. Starting RNA was made from brain tissue removed from a Caucasian male fetus, who was stillborn with a hypoplastic left heart at 23 weeks' gestation. The library was normalized in 2 rounds using conditions adapted from Soares et al., PNAS (1994) 91: 9228 and Bonaldo et al., Genome Research (1996) 6: 791, except that a significantly longer (48 hours/round) reannealing hybridization was used. BRAIFEN05 pINCY This normalized fetal brain tissue library was constructed from 3.26 million independent clones from a fetal brain library. Starting RNA was made from brain tissue removed from a Caucasian male fetus, who was stillborn with a hypoplastic left heart at 23 weeks' gestation. The library was normalized in 2 rounds using conditions adapted from Soares et al., PNAS (1994) 91: 9228 and Bonaldo et al., Genome Research (1996) 6: 791, except that a significantly longer (48 hours/round) reannealing hybridization was used. BRAINOT14 pINCY Library was constructed using RNA isolated from brain tissue removed from the left frontal lobe of a 40-year-old Caucasian female during excision of a cerebral meningeal lesion. Pathology for the associated tumor tissue indicated grade 4 gemistocytic astrocytoma. BRAITUT02 PSPORT1 Library was constructed using RNA isolated from brain tumor tissue removed from the frontal lobe of a 58-year-old Caucasian male during excision of a cerebral meningeal lesion. Pathology indicated a grade 2 metastatic hypernephroma. Patient history included a grade 2 renal cell carcinoma, insomnia, and chronic airway obstruction. Family history included a malignant neoplasm of the kidney. BRAITUT03 PSPORT1 Library was constructed using RNA isolated from brain tumor tissue removed from the left frontal lobe of a 17-year-old Caucasian female during excision of a cerebral meningeal lesion. Pathology indicated a grade 4 fibrillary giant and small-cell astrocytoma. Family history included benign hypertension and cerebrovascular disease. BRSTNOT02 PSPORT1 Library was constructed using RNA isolated from diseased breast tissue removed from a 55-year-old Caucasian female during a unilateral extended simple mastectomy. Pathology indicated proliferative fibrocysytic changes characterized by apocrine metaplasia, sclerosing adenosis, cyst formation, and ductal hyperplasia without atypia. Pathology for the associated tumor tissue indicated an invasive grade 4 mammary adenocarcinoma. Patient history included atrial tachycardia and a benign neoplasm. Family history included cardiovascular and cerebrovascular disease. BRSTTUT01 PSPORT1 Library was constructed using RNA isolated from breast tumor tissue removed from a 55-year-old Caucasian female during a unilateral extended simple mastectomy. Pathology indicated invasive grade 4 mammary adenocarcinoma of mixed lobular and ductal type, extensively involving the left breast. The tumor was identified in the deep dermis near the lactiferous ducts with extracapsular extension. Seven mid and low and five high axillary lymph nodes were positive for tumor. Proliferative fibrocysytic changes were characterized by apocrine metaplasia, sclerosing adenosis, cyst formation, and ductal hyperplasia without atypia. Patient history included atrial tachycardia, blood in the stool, and a benign breast neoplasm. Family history included benign hypertension, atherosclerotic coronary artery disease, cerebrovascular disease, and depressive disorder. COLNFET02 pINCY Library was constructed using RNA isolated from the colon tissue of a Caucasian female fetus, who died at 20 weeks' gestation. COLNNOT11 PSPORT1 Library was constructed using RNA isolated from colon tissue removed from a 60- year-old Caucasian male during a left hemicolectomy. ENDANOT01 PBLUESCRIPT Library was constructed using RNA isolated from aortic endothelial cell tissue from an explanted heart removed from a male during a heart transplant. ENDCNON02 pINCY This normalized coronary artery endothelial cell tissue library was constructed from 444,000 independent clones from an endothelial tissue library. Starting RNA was made from coronary artery endothelial cell tissue removed from a 3-year-old Caucasian male. This library was normalized in two rounds using conditions adapted from Soares et al., (PNAS (1994) 91: 9228-9232) and Bonaldo et al., (Genome Research (1996) 6: 791-806), using a significantly longer (48 hours/round) reannealing hybridization period. EPIPNON05 pINCY This normalized prostate epithelial cell tissue library was constructed from 2.36 million independent clones from a prostate epithelial cell tissue library. Starting RNA was made from untreated prostatic epithelial cell issue removed from a 17-year- old Hispanic male. The library was normalized in two rounds using conditions adapted from Soares et al., PNAS (1994) 91: 9228 and Bonaldo et al., Genome Research (1996) 6: 791, except that a significantly longer (48 -hours/round) reannealing hybridization was used. HNT2RAT01 PBLUESCRIPT Library was constructed at Stratagene (STR937231), using RNA isolated from the hNT2 cell line (derived from a human teratocarcinoma that exhibited properties characteristic of a committed neuronal precursor). Cells were treated with retinoic acid for 24 hours ISLTNOT01 pINCY Library was constructed using RNA isolated from a pooled collection of pancreatic islet cells. KERANOT01 PBLUESCRIPT Library was constructed using RNA isolated from neonatal keratinocytes obtained from the leg skin of a spontaneously aborted black male. KIDNNOT05 PSPORT1 Library was constructed using RNA isolated from the kidney tissue of a 2-day-old Hispanic female, who died from cerebral anoxia. Family history included congenital heart disease. KIDNNOT09 pINCY Library was constructed using RNA isolated from the kidney tissue of a Caucasian male fetus, who died at 23 weeks' gestation. KIDNTUT01 PSPORT1 Library was constructed using RNA isolated from the kidney tumor tissue removed from an 8-month-old female during nephroureterectomy. Pathology indicated Wilms' tumor (nephroblastoma), which involved 90 percent of the renal parenchyma. Prior to surgery, the patient was receiving heparin anticoagulant therapy. LIVRNON08 pINCY This normalized library was constructed from 5.7 million independent clones from a pooled liver tissue library. Starting RNA was made from pooled liver tissue removed from a 4-year-old Hispanic male who died from anoxia and a 16 week female fetus who died after 16-weeks gestation from anencephaly. Serologies were positive for cytolomegalovirus in the 4-year-old. Patient history included asthma in the 4- year-old. Family history included taking daily prenatal vitamins and mitral valve prolapse in the mother of the fetus. The library was normalized in 2 rounds using conditions adapted from Soares et al., PNAS (1994) 91: 9228 and Bonaldo et al., Genome Research 6 (1996): 791, except that a significantly longer (48 hours/round) reannealing hybridization was used. LNODNOT03 pINCY Library was constructed using RNA isolated from lymph node tissue obtained from a 67-year-old Caucasian male during a segmental lung resection and bronchoscopy. On microscopic exam, this tissue was found to be extensively necrotic with 10% viable tumor. Pathology for the associated tumor tissue indicated invasive grade 3-4 squamous cell carcinoma. Patient history included hemangioma. Family history included atherosclerotic coronary artery disease, benign hypertension, congestive heart failure, atherosclerotic coronary artery disease. LUNGNOT14 pINCY Library was constructed, using RNA isolated from lung tissue removed from the left lower lobe of a 47-year-old Caucasian male during a segmental lung resection. Pathology for the associated tumor tissue indicated a grade 4 adenocarcinoma, and the parenchyma showed calcified granuloma. Patient history included benign hypertension and chronic obstructive pulmonary disease. Family history included type II diabetes and acute myocardial infarction. LUNGNOT20 pINCY Library was constructed using RNA isolated from right upper lobe lung tissue removed from a 61-year-old Caucasian male. Pathology indicated panacinal emphysema with blebs in the right anterior upper lobe and apex, as well as emphysema in the right posterior upper lobe. Patient history included angina pectoris, and gastric ulcer. Family history included a subdural hemorrhage, cancer of an unidentified site, atherosclerotic coronary artery disease, and pneumonia. LUNGNOT27 pINCY Library was constructed using RNA isolated from lung tissue removed from a 17-year- old Hispanic female. LUTGTUT03 PSPORT1 Library was constructed using RNA isolated from lung tumor tissue removed from the left lower lobe of a 69-year-old Caucasian male during segmental lung resection. Pathology indicated residual grade 3 invasive squamous cell carcinoma. Patient history included acute myocardial infarction, prostatic hyperplasia, malignant skin neoplasm, and tobacco use. LUNGTUT09 pINCY Library was constructed using RNA isolated from lung tumor tissue removed from a 68-year-old Caucasian male during segmental lung resection. Pathology indicated invasive grade 3 squamous cell carcinoma and a metastatic tumor. Patient history included type II diabetes, thyroid disorder, depressive disorder, hyperlipidemia, esophageal ulcer, and tobacco use. MENITUT03 pINCY Library was constructed using RNA isolated from brain meningioma tissue removed from a 35-year-old Caucasian female during excision of a cerebral meningeal lesion. Pathology indicated a benign neoplasm in the right cerebellopontine angle of the brain. Patient history included hypothyroidism. Family history included myocardial infarction and breast cancer. OVARNOT03 PSPORT1 Library was constructed using RNA isolated from ovarian tissue removed from a 43- year-old Caucasian female during removal of the fallopian tubes and ovaries. Pathology for the associated tumor tissue indicated grade 2 mucinous cystadenocarcinoma. Patient history included mitral valve disorder, pneumonia, and viral hepatitis. Family history included atherosclerotic coronary artery disease, pancreatic cancer, stress reaction, cerebrovascular disease, breast cancer, and uterine cancer. OVARTUT01 PSPORT1 Library was constructed using RNA isolated from ovarian tumor tissue removed from a 43-year-old Caucasian female during removal of the fallopian tubes and ovaries. Pathology indicated grade 2 mucinous cystadenocarcinoma involving the entire left ovary. Patient history included mitral valve disorder, pneumonia, and viral hepatitis. Family history included atherosclerotic coronary artery disease, pancreatic cancer, stress reaction, cerebrovascular disease, breast cancer, and uterine cancer. PANCNOT07 pINCY Library was constructed using RNA isolated from the pancreatic tissue of a Caucasian male fetus, who died at 23 weeks' gestation. PANCNOT08 pINCY Library was constructed using RNA isolated from pancreatic tissue removed from a 65-year-old Caucasian female during radical subtotal pancreatectomy. Pathology for the associated tumor tissue indicated an invasive grade 2 adenocarcinoma. Patient history included type II diabetes, osteoarthritis, cardiovascular disease, benign neoplasm in the large bowel, and a cataract. Previous surgeries included a total splenectomy, cholecystectomy, and abdominal hysterectomy. Family history included cardiovascular disease, type II diabetes, and stomach cancer. PITUNOT01 PBLUESCRIPT Library was constructed using RNA obtained from Clontech (CLON 6584-2, lot 35278). The RNA was isolated from the pituitary glands removed from a pool of 18 male and female Caucasian donors, 16 to 70 years old, who died from trauma. PROSNOT16 pINCY Library was constructed using RNA isolated from diseased prostate tissue removed from a 68-year-old Caucasian male during a radical prostatectomy. Pathology indicated adenofibromatous hyperplasia. Pathology for the associated tumor tissue indicated an adenocarcinoma (Gleason grade 3 + 4). The patient presented with elevated prostate specific antigen (PSA). During this hospitalization, the patient was diagnosed with myasthenia gravis. Patient history included osteoarthritis, and type II diabetes. Family history included benign hypertension, acute myocardial infarction, hyperlipidemia, and arteriosclerotic coronary artery disease. SINTFET03 pINCY Library was constructed using RNA isolated from small intestine tissue removed from a Caucasian female fetus, who died at 20 weeks' gestation. SPLNFET01 PBLUESCRIPT Library was constructed at Stratagene, using RNA isolated from a pool of fetal spleen tissue. Following vector packaging, 2 million primary clones were then amplified to stabilize the library for long-term storage. Amplification may significantly skew sequence abundances. SPLNNOT04 pINCY Library was constructed using RNA isolated from the spleen tissue of a 2-year-old Hispanic male, who died from cerebral anoxia. Past medical history and serologies were negative. THP1NOT03 pINCY Library was constructed using 1 microgram of polyA RNA isolated from untreated THP- 1 cells. THP-1 (ATCC TIB 202) is a human promonocyte line derived from the peripheral blood of a 1-year-old Caucasian male with acute monocytic leukemia (ref: Int. J. Cancer (1980) 26: 171). TLYMNOT02 PBLUESCRIPT Library was constructed using RNA isolated from non-adherent peripheral blood mononuclear cells. The blood was obtained from unrelated male and female donors. Cells from each donor were purified on Ficoll Hypaque, then harvested by centrifugation, lysed in a buffer containing GuSCN, and spun through CsCl to obtain RNA for library construction. UCMCL5T01 PBLUESCRIPT Library was constructed using RNA isolated from mononuclear cells obtained from the umbilical cord blood of 12 individuals. The cells were cultured for 12 days with IL-5 before RNA was obtained from the pooled lysates. UTRSNOT05 pINCY The library was constructed using RNA isolated from the uterine tissue of a 45- year-old Caucasian female during a total abdominal hysterectomy and total colectomy. Pathology for the associated tumor tissue indicated multiple leiomyomas of the myometrium and a grade 2 colonic adenocarcinoma of the cecum. Patient history included multiple sclerosis and mitral valve disorder. Family history included type I diabetes, cerebrovascular disease, atherosclerotic coronary artery disease, malignant skin neoplasm, hypertension, and malignant neoplasm of the colon.

[0369] TABLE 7 Parameter Program Description Reference Threshold ABI A program that removes vector sequences and Applied Biosystems, Foster City, CA. FACTURA masks ambiguous bases in nucleic acid sequences. ABI/ A Fast Data Finder useful in comparing and Applied Biosystems, Foster City, CA; Mismatch PARACEL annotating amino acid or nucleic acid sequences. Paracel Inc., Pasadena, CA. <50% FDF ABI A program that assembles nucleic acid sequences. Applied Biosystems, Foster City, CA. AutoAssembler BLAST A Basic Local Alignment Search Tool useful in Altschul, S. F. et al. (1990) J. Mol. Biol. ESTs: sequence similarity search for amino acid and 215: 403-410; Altschul, S. F. et al. (1997) Probability nucleic acid sequences. BLAST includes five Nucleic Acids Res. 25: 3389-3402. value = 1.0E−8 functions: blastp, blastn, blastx, tblastn, and tblastx. or less Full Length sequences: Probability value = 1.0E−10 or less FASTA A Pearson and Lipman algorithm that searches for Pearson, W. R. and D. J. Lipman (1988) Proc. ESTs: fasta E similarity between a query sequence and a group of Natl. Acad Sci. USA 85: 2444-2448; Pearson, value = sequences of the same type. FASTA comprises as W. R. (1990) Methods Enzymol. 183: 63-98; 1.06E−6 least five functions: fasta, tfasta, fastx, tfastx, and and Smith, T. F. and M. S. Waterman (1981) Assembled ssearch. Adv. Appl. Math. 2: 482-489. ESTs: fasta Identity = 95% or greater and Match length = 200 bases or greater; fastx E value = 1.0E−8 or less Full Length sequences: fastx score = 100 or greater BLIMPS A BLocks IMProved Searcher that matches a Henikoff, S. and J. G. Henikoff (1991) Nucleic Probability sequence against those in BLOCKS, PRINTS, Acids Res. 19: 6565-6572; Henikoff, J. G. and value = 1.0E−3 DOMO, PRODOM, and PFAM databases to search S. Henikoff (1996) Methods Enzymol. or less for gene families, sequence homology, and structural 266: 88-105; and Attwood, T. K. et al. (1997) J. fingerprint regions. Chem. Inf. Comput. Sci. 37: 417-424. HMMER An algorithm for searching a query sequence against Krogh, A. et al. (1994) J. Mol. Biol. PFAM hits: hidden Markov model (HMM)-based databases of 235: 1501-1531; Sonnhammer, E. L. L. et al. Probability protein family consensus sequences, such as PFAM. (1988) Nucleic Acids Res. 26: 320-322; value = 1.0E−3 Durbin, R. et al. (1998) Our World View, in a or less Nutshell, Cambridge Univ. Press, pp. 1-350. Signal peptide hits: Score = 0 or greater ProfileScan An algorithm that searches for structural and sequence Gribskov, M. et al. (1988) CABIOS 4: 61-66; Normalized motifs in protein sequences that match sequence patterns Gribskov, M. et al. (1989) Methods Enzymol. quality score ≧ defined in Prosite. 183: 146-159; Bairoch, A. et al. (1997) GCG-specified Nucleic Acids Res. 25: 217-221. “HIGH” value for that particular Prosite motif. Generally, score = 1.4-2.1. Phred A base-calling algorithm that examines automated Ewing, B. et al. (1998) Genome Res. sequencer traces with high sensitivity and probability. 8: 175-185; Ewing, B. and P. Green (1998) Genome Res. 8: 186-194. Phrap A Phils Revised Assembly Program including SWAT and Smith, T. F. and M. S. Waterman (1981) Adv. Score = 120 or CrossMatch, programs based on efficient implementation Appl. Math. 2: 482-489; Smith, T.F. and M.S. greater; of the Smith-Waterman algorithm, useful in searching Waterman (1981) J. Mol. Biol. 147: 195-197; Match length = sequence homology and assembling DNA sequences. and Green, P., University of Washington, 56 or greater Seattle, WA. Consed A graphical tool for viewing and editing Phrap assemblies. Gordon, D. et al. (1998) Genome Res. 8: 195-202. SPScan A weight matrix analysis program that scans protein Nielson, H. et al. (1997) Protein Engineering Score = 3.5 or sequences for the presence of secretory signal peptides. 10: 1-6; Claverie, J.M. and S. Audic (1997) greater CABIOS 12: 431-439. TMAP A program that uses weight matrices to delineate Persson, B. and P. Argos (1994) J. Mol. Biol. transmembrane segments on protein sequences and 237: 182-192; Persson, B. and P. Argos (1996) determine orientation. Protein Sci. 5: 363-371. TMHMMER A program that uses a hidden Markov model (HMM) to Sonnhammer, E. L. et al. (1998) Proc. Sixth Intl. delineate transmembrane segments on protein sequences Conf. on Intelligent Systems for Mol. Biol., and determine orientation. Glasgow et al., eds., The Am. Assoc. for Artificial Intelligence Press, Menlo Park, CA, pp. 175-182. Motifs A program that searches amino acid sequences for patterns Bairoch, A. et al. (1997) Nucleic Acids that matched those defined in Prosite. Res. 25: 217-221; Wisconsin Package Program Manual, version 9, page M51-59, Genetics Computer Group, Madison, WI.

[0370]

1 94 1 245 PRT Homo sapiens misc_feature Incyte ID No 1622129CD1 1 Met Ala Gly Leu Glu Leu Leu Ser Asp Gln Gly Tyr Arg Val Asp 1 5 10 15 Gly Arg Arg Ala Gly Glu Leu Arg Lys Ile Gln Ala Arg Met Gly 20 25 30 Val Phe Ala Gln Ala Asp Gly Ser Ala Tyr Ile Glu Gln Gly Asn 35 40 45 Thr Lys Ala Leu Ala Val Val Tyr Gly Pro His Glu Ile Arg Gly 50 55 60 Ser Arg Ala Arg Ala Leu Pro Asp Arg Ala Leu Val Asn Cys Gln 65 70 75 Tyr Ser Ser Ala Thr Phe Ser Thr Gly Glu Arg Lys Arg Arg Pro 80 85 90 His Gly Asp Arg Lys Ser Cys Glu Met Gly Leu Gln Leu Arg Gln 95 100 105 Thr Phe Glu Ala Ala Ile Leu Thr Gln Leu His Pro Arg Ser Gln 110 115 120 Ile Asp Ile Tyr Val Gln Val Leu Gln Ala Asp Gly Gly Thr Tyr 125 130 135 Ala Ala Cys Val Asn Ala Ala Thr Leu Ala Val Leu Asp Ala Gly 140 145 150 Ile Pro Met Arg Asp Phe Val Cys Ala Cys Ser Ala Gly Phe Val 155 160 165 Asp Gly Thr Ala Leu Ala Asp Leu Ser His Val Glu Glu Ala Ala 170 175 180 Gly Gly Pro Gln Leu Ala Leu Ala Leu Leu Pro Ala Ser Gly Gln 185 190 195 Ile Ala Leu Leu Glu Met Asp Ala Arg Leu His Glu Asp His Leu 200 205 210 Glu Arg Val Leu Glu Ala Ala Ala Gln Ala Ala Arg Asp Val His 215 220 225 Thr Leu Leu Asp Arg Val Val Arg Gln His Val Arg Glu Ala Ser 230 235 240 Ile Leu Leu Gly Asp 245 2 118 PRT Homo sapiens misc_feature Incyte ID No 1820078CD1 2 Met Thr Asp Thr Ala Glu Ala Val Pro Lys Phe Glu Glu Met Phe 1 5 10 15 Ala Ser Arg Phe Thr Glu Asn Asp Lys Glu Tyr Gln Glu Tyr Leu 20 25 30 Lys Arg Pro Pro Glu Ser Pro Pro Ile Val Glu Glu Trp Asn Ser 35 40 45 Arg Ala Gly Gly Asn Gln Arg Asn Arg Gly Asn Arg Leu Gln Asp 50 55 60 Asn Arg Gln Phe Arg Gly Arg Asp Asn Arg Trp Gly Trp Pro Ser 65 70 75 Asp Asn Arg Ser Asn Gln Trp His Gly Arg Ser Trp Gly Asn Asn 80 85 90 Tyr Pro Gln His Arg Gln Glu Pro Tyr Tyr Pro Gln Gln Tyr Gly 95 100 105 His Tyr Gly Tyr Asn Gln Arg Pro Pro Tyr Gly Tyr Tyr 110 115 3 179 PRT Homo sapiens misc_feature Incyte ID No 1527017CD1 3 Met Phe Gly Ser Ser Arg Arg Leu Ser Ser Ser Lys Leu Leu Gln 1 5 10 15 Gln Gly Lys Thr Ser Ser Val Phe Glu Asp Pro Val Ile Ser Lys 20 25 30 Phe Thr Asn Met Met Met Ile Gly Gly Asn Lys Val Leu Ala Arg 35 40 45 Ser Leu Met Ile Gln Thr Leu Glu Ala Val Lys Arg Lys Gln Phe 50 55 60 Glu Lys Tyr His Ala Ala Ser Ala Glu Glu Gln Ala Thr Ile Glu 65 70 75 Arg Asn Pro Tyr Thr Ile Phe His Gln Ala Leu Lys Asn Cys Glu 80 85 90 Pro Met Ile Gly Leu Val Pro Ile Leu Lys Gly Gly Arg Phe Tyr 95 100 105 Gln Val Pro Val Pro Leu Pro Asp Arg Arg Arg Arg Phe Leu Ala 110 115 120 Met Lys Trp Met Ile Thr Glu Cys Arg Asp Lys Lys His Gln Arg 125 130 135 Thr Leu Met Pro Glu Lys Leu Ser His Lys Leu Leu Glu Ala Phe 140 145 150 His Asn Gln Gly Pro Val Ile Lys Arg Lys His Asp Leu His Lys 155 160 165 Met Ala Glu Ala Asn Arg Ala Leu Ala His Tyr Arg Trp Trp 170 175 4 101 PRT Homo sapiens misc_feature Incyte ID No 1647264CD1 4 Met Glu Arg Pro Asp Lys Ala Ala Leu Asn Ala Leu Gln Pro Pro 1 5 10 15 Glu Phe Arg Asn Glu Ser Ser Leu Ala Ser Thr Leu Lys Thr Leu 20 25 30 Leu Phe Phe Thr Ala Leu Met Ile Thr Val Pro Ile Gly Leu Tyr 35 40 45 Phe Thr Thr Lys Ser Tyr Ile Phe Glu Gly Ala Leu Gly Met Ser 50 55 60 Asn Arg Asp Ser Tyr Phe Tyr Ala Ala Ile Val Ala Val Val Ala 65 70 75 Val His Val Val Leu Ala Leu Phe Val Tyr Val Ala Trp Asn Glu 80 85 90 Gly Ser Arg Gln Trp Arg Glu Gly Lys Gln Asp 95 100 5 145 PRT Homo sapiens misc_feature Incyte ID No 1721989CD1 5 Met Ala Phe Phe Thr Gly Leu Trp Gly Pro Phe Thr Cys Val Ser 1 5 10 15 Arg Val Leu Ser His His Cys Phe Ser Thr Thr Gly Ser Leu Ser 20 25 30 Ala Ile Gln Lys Met Thr Arg Val Arg Val Val Asp Asn Ser Ala 35 40 45 Leu Gly Asn Ser Pro Tyr His Arg Ala Pro Arg Cys Ile His Val 50 55 60 Tyr Lys Lys Asn Gly Val Gly Lys Val Gly Asp Gln Ile Leu Leu 65 70 75 Ala Ile Lys Gly Gln Lys Lys Lys Ala Leu Ile Val Gly His Cys 80 85 90 Met Pro Gly Pro Arg Met Thr Pro Arg Phe Asp Ser Asn Asn Val 95 100 105 Val Leu Ile Glu Asp Asn Gly Asn Pro Val Gly Thr Arg Ile Lys 110 115 120 Thr Pro Ile Pro Thr Ser Leu Arg Lys Arg Glu Gly Glu Tyr Ser 125 130 135 Lys Val Leu Ala Ile Ala Gln Asn Phe Val 140 145 6 249 PRT Homo sapiens misc_feature Incyte ID No 1730581CD1 6 Met Ala Ala Gln Ser Ala Pro Lys Val Val Leu Lys Ser Thr Thr 1 5 10 15 Lys Met Ser Leu Asn Glu Arg Phe Thr Asn Met Leu Lys Asn Lys 20 25 30 Gln Pro Thr Pro Val Asn Ile Arg Ala Ser Met Gln Gln Gln Gln 35 40 45 Gln Leu Ala Ser Ala Arg Asn Arg Arg Leu Ala Gln Gln Met Glu 50 55 60 Asn Arg Pro Ser Val Gln Ala Ala Leu Lys Leu Lys Gln Lys Ser 65 70 75 Leu Lys Gln Arg Leu Gly Lys Ser Asn Ile Gln Ala Arg Leu Gly 80 85 90 Arg Pro Ile Gly Ala Leu Ala Arg Gly Ala Ile Gly Gly Arg Gly 95 100 105 Leu Pro Ile Ile Gln Arg Gly Leu Pro Arg Gly Gly Leu Arg Gly 110 115 120 Gly Arg Ala Thr Arg Thr Leu Leu Arg Gly Gly Met Ser Leu Arg 125 130 135 Gly Gln Asn Leu Leu Arg Gly Gly Arg Ala Val Ala Pro Arg Met 140 145 150 Gly Leu Arg Arg Gly Gly Val Arg Gly Arg Gly Gly Pro Gly Arg 155 160 165 Gly Gly Leu Gly Arg Gly Ala Met Gly Arg Gly Gly Ile Gly Gly 170 175 180 Arg Gly Arg Gly Met Ile Gly Arg Gly Arg Gly Gly Phe Gly Gly 185 190 195 Arg Gly Arg Gly Arg Gly Arg Gly Arg Gly Ala Leu Ala Arg Pro 200 205 210 Val Leu Thr Lys Glu Gln Leu Asp Asn Gln Leu Asp Ala Tyr Met 215 220 225 Ser Lys Thr Lys Gly His Leu Asp Ala Glu Leu Asp Ala Tyr Met 230 235 240 Ala Gln Thr Asp Pro Glu Thr Asn Asp 245 7 265 PRT Homo sapiens misc_feature Incyte ID No 1740714CD1 7 Met Arg Arg Ala Glu Leu Ala Gly Leu Lys Thr Met Ala Trp Val 1 5 10 15 Pro Ala Glu Ser Ala Val Glu Glu Leu Met Pro Arg Leu Leu Pro 20 25 30 Val Glu Pro Cys Asp Leu Thr Glu Gly Phe Asp Pro Ser Val Pro 35 40 45 Pro Arg Thr Pro Gln Glu Tyr Leu Arg Arg Val Gln Ile Glu Ala 50 55 60 Ala Gln Cys Pro Asp Val Val Val Ala Gln Ile Asp Pro Lys Lys 65 70 75 Leu Lys Arg Lys Gln Ser Val Asn Ile Ser Leu Ser Gly Cys Gln 80 85 90 Pro Ala Pro Glu Gly Tyr Ser Pro Thr Leu Gln Trp Gln Gln Gln 95 100 105 Gln Val Ala Gln Phe Ser Thr Val Arg Gln Asn Val Asn Lys His 110 115 120 Arg Ser His Trp Lys Ser Gln Gln Leu Asp Ser Asn Val Thr Met 125 130 135 Pro Lys Ser Glu Asp Glu Glu Gly Trp Lys Lys Phe Cys Leu Gly 140 145 150 Glu Lys Leu Cys Ala Asp Gly Ala Val Gly Pro Ala Thr Asn Glu 155 160 165 Ser Pro Gly Ile Asp Tyr Val Gln Ala Thr Val Thr Ser Val Leu 170 175 180 Glu Tyr Leu Ser Asn Trp Phe Gly Glu Arg Asp Phe Thr Pro Glu 185 190 195 Leu Gly Arg Trp Leu Tyr Ala Leu Leu Ala Cys Leu Glu Lys Pro 200 205 210 Leu Leu Pro Glu Ala His Ser Leu Ile Arg Gln Leu Ala Arg Arg 215 220 225 Cys Ser Glu Val Arg Leu Leu Val Asp Ser Lys Asp Asp Glu Arg 230 235 240 Val Pro Ala Leu Asn Leu Leu Ile Cys Leu Val Ser Arg Tyr Phe 245 250 255 Asp Gln Arg Asp Leu Ala Asp Glu Pro Ser 260 265 8 306 PRT Homo sapiens misc_feature Incyte ID No 1850596CD1 8 Met Ser Leu Lys Leu Gln Ala Ser Asn Val Thr Asn Lys Asn Asp 1 5 10 15 Pro Lys Ser Ile Asn Ser Arg Val Phe Ile Gly Asn Leu Asn Thr 20 25 30 Ala Leu Val Lys Lys Ser Asp Val Glu Thr Ile Phe Ser Lys Tyr 35 40 45 Gly Arg Val Ala Gly Cys Ser Val His Lys Gly Tyr Ala Phe Val 50 55 60 Gln Tyr Ser Asn Glu Arg His Ala Arg Ala Ala Val Leu Gly Glu 65 70 75 Asn Gly Arg Val Leu Ala Gly Gln Thr Leu Asp Ile Asn Met Ala 80 85 90 Gly Glu Pro Lys Pro Asp Arg Pro Lys Gly Leu Lys Arg Ala Ala 95 100 105 Ser Ala Ile Tyr Ser Gly Tyr Ile Phe Asp Tyr Asp Tyr Tyr Arg 110 115 120 Asp Asp Phe Tyr Asp Arg Leu Phe Asp Tyr Arg Gly Arg Leu Ser 125 130 135 Pro Val Pro Val Pro Arg Ala Val Pro Val Lys Arg Pro Arg Val 140 145 150 Thr Val Pro Leu Val Arg Arg Val Lys Thr Asn Val Pro Val Lys 155 160 165 Leu Phe Ala Arg Ser Thr Ala Val Thr Thr Ser Ser Ala Lys Ile 170 175 180 Lys Leu Lys Ser Ser Glu Leu Gln Ala Ile Lys Thr Glu Leu Thr 185 190 195 Gln Ile Lys Ser Asn Ile Asp Ala Leu Leu Ser Arg Leu Glu Gln 200 205 210 Ile Ala Ala Glu Gln Lys Ala Asn Pro Asp Gly Lys Lys Lys Gly 215 220 225 Asp Gly Gly Gly Ala Gly Gly Gly Gly Gly Gly Gly Gly Ser Gly 230 235 240 Gly Gly Gly Ser Gly Gly Gly Gly Gly Gly Gly Ser Ser Arg Pro 245 250 255 Pro Ala Pro Gln Glu Asn Thr Thr Ser Glu Ala Gly Leu Pro Gln 260 265 270 Gly Glu Ala Arg Thr Arg Asp Asp Gly Asp Glu Glu Gly Leu Leu 275 280 285 Thr His Ser Glu Glu Glu Leu Glu His Ser Gln Asp Thr Asp Ala 290 295 300 Asp Asp Gly Ala Leu Gln 305 9 332 PRT Homo sapiens misc_feature Incyte ID No 1856109CD1 9 Met Ala Ser Gly Leu Val Arg Leu Leu Gln Gln Gly His Arg Cys 1 5 10 15 Leu Leu Ala Pro Val Ala Pro Lys Leu Val Pro Pro Val Arg Gly 20 25 30 Val Lys Lys Gly Phe Arg Ala Ala Phe Arg Phe Gln Lys Glu Leu 35 40 45 Glu Arg Gln Arg Leu Leu Arg Cys Pro Pro Pro Pro Val Arg Arg 50 55 60 Ser Glu Lys Pro Asn Trp Asp Tyr His Ala Glu Ile Gln Ala Phe 65 70 75 Gly His Arg Leu Gln Glu Asn Phe Ser Leu Asp Leu Leu Lys Thr 80 85 90 Ala Phe Val Asn Ser Cys Tyr Ile Lys Ser Glu Glu Ala Lys Arg 95 100 105 Gln Gln Leu Gly Ile Glu Lys Glu Ala Val Leu Leu Asn Leu Lys 110 115 120 Ser Asn Gln Glu Leu Ser Glu Gln Gly Thr Ser Phe Ser Gln Thr 125 130 135 Cys Leu Thr Gln Phe Leu Glu Asp Glu Tyr Pro Asp Met Pro Thr 140 145 150 Glu Gly Ile Lys Asn Leu Val Asp Phe Leu Thr Gly Glu Glu Val 155 160 165 Val Cys His Val Ala Arg Asn Leu Ala Val Glu Gln Leu Thr Leu 170 175 180 Ser Glu Glu Phe Pro Val Pro Pro Ala Val Leu Gln Gln Thr Phe 185 190 195 Phe Ala Val Ile Gly Ala Leu Leu Gln Ser Ser Gly Pro Glu Arg 200 205 210 Thr Ala Leu Phe Ile Arg Asp Phe Leu Ile Thr Gln Met Thr Gly 215 220 225 Lys Glu Leu Phe Glu Met Trp Lys Ile Ile Asn Pro Met Gly Leu 230 235 240 Leu Val Glu Glu Leu Lys Lys Arg Asn Val Ser Ala Pro Glu Ser 245 250 255 Arg Leu Thr Arg Gln Ser Gly Gly Thr Thr Ala Leu Pro Leu Tyr 260 265 270 Phe Val Gly Leu Tyr Cys Asp Lys Lys Leu Ile Ala Glu Gly Pro 275 280 285 Gly Glu Thr Val Leu Val Ala Glu Glu Glu Ala Ala Arg Val Ala 290 295 300 Leu Arg Lys Leu Tyr Gly Phe Thr Glu Asn Arg Arg Pro Trp Asn 305 310 315 Tyr Ser Lys Pro Lys Glu Thr Leu Arg Ala Glu Lys Ser Ile Thr 320 325 330 Ala Ser 10 279 PRT Homo sapiens misc_feature Incyte ID No 1921719CD1 10 Met Ala Ala Pro Val Arg Arg Thr Leu Leu Gly Val Ala Gly Gly 1 5 10 15 Trp Arg Arg Phe Glu Arg Leu Trp Ala Gly Ser Leu Ser Ser Arg 20 25 30 Ser Leu Ala Leu Ala Ala Ala Pro Ser Ser Asn Gly Ser Pro Trp 35 40 45 Arg Leu Leu Gly Ala Leu Cys Leu Gln Arg Pro Pro Val Val Ser 50 55 60 Lys Pro Leu Thr Pro Leu Gln Glu Glu Met Ala Ser Leu Leu Gln 65 70 75 Gln Ile Glu Ile Glu Arg Ser Leu Tyr Ser Asp His Glu Leu Arg 80 85 90 Ala Leu Asp Glu Asn Gln Arg Leu Ala Lys Lys Lys Ala Asp Leu 95 100 105 His Asp Glu Glu Asp Glu Gln Asp Ile Leu Leu Ala Gln Asp Leu 110 115 120 Glu Asp Met Trp Glu Gln Lys Phe Leu Gln Phe Lys Leu Gly Ala 125 130 135 Arg Ile Thr Glu Ala Asp Glu Lys Asn Asp Arg Thr Ser Leu Asn 140 145 150 Arg Lys Leu Asp Arg Asn Leu Val Leu Leu Val Arg Glu Lys Phe 155 160 165 Gly Asp Gln Asp Val Trp Ile Leu Pro Gln Ala Glu Trp Gln Pro 170 175 180 Gly Glu Thr Leu Arg Gly Thr Ala Glu Arg Thr Leu Ala Thr Leu 185 190 195 Ser Glu Asn Asn Met Glu Ala Lys Phe Leu Gly Asn Ala Pro Cys 200 205 210 Gly His Tyr Thr Phe Lys Phe Pro Gln Ala Met Arg Thr Glu Ser 215 220 225 Asn Leu Gly Ala Lys Val Phe Phe Phe Lys Ala Leu Leu Leu Thr 230 235 240 Gly Asp Phe Ser Gln Ala Gly Asn Lys Gly His His Val Trp Val 245 250 255 Thr Lys Asp Glu Leu Gly Asp Tyr Leu Lys Pro Lys Tyr Leu Ala 260 265 270 Gln Val Arg Arg Phe Val Ser Asp Leu 275 11 239 PRT Homo sapiens misc_feature Incyte ID No 2099829CD1 11 Met Pro Lys Ser Lys Arg Asp Lys Lys Val Ser Leu Thr Lys Thr 1 5 10 15 Ala Lys Lys Gly Leu Glu Leu Lys Gln Asn Leu Ile Glu Glu Leu 20 25 30 Arg Lys Cys Val Asp Thr Tyr Lys Tyr Leu Phe Ile Phe Ser Val 35 40 45 Ala Asn Met Arg Asn Ser Lys Leu Lys Asp Ile Arg Asn Ala Trp 50 55 60 Lys His Ser Arg Met Phe Phe Gly Lys Asn Lys Val Met Met Val 65 70 75 Ala Leu Gly Arg Ser Pro Ser Asp Glu Tyr Lys Asp Asn Leu His 80 85 90 Gln Val Ser Lys Arg Leu Arg Gly Glu Val Gly Leu Leu Phe Thr 95 100 105 Asn Arg Thr Lys Glu Glu Val Asn Glu Trp Phe Thr Lys Tyr Thr 110 115 120 Glu Met Asp Tyr Ala Arg Ala Gly Asn Lys Ala Ala Phe Thr Val 125 130 135 Ser Leu Asp Pro Gly Pro Leu Glu Gln Phe Pro His Ser Met Glu 140 145 150 Pro Gln Leu Arg Gln Leu Gly Leu Pro Thr Ala Leu Lys Arg Gly 155 160 165 Val Val Thr Leu Leu Ser Asp Tyr Glu Val Cys Lys Glu Gly Asp 170 175 180 Val Leu Thr Pro Glu Gln Ala Arg Val Leu Lys Leu Phe Gly Tyr 185 190 195 Glu Met Ala Glu Phe Lys Val Thr Ile Lys Tyr Met Trp Asp Ser 200 205 210 Gln Ser Gly Arg Phe Gln Gln Met Gly Asp Asp Leu Pro Glu Ser 215 220 225 Ala Ser Glu Ser Thr Glu Glu Ser Asp Ser Glu Asp Asp Asp 230 235 12 291 PRT Homo sapiens misc_feature Incyte ID No 2416915CD1 12 Met Asp Phe Glu Asn Leu Phe Ser Lys Pro Pro Asn Pro Ala Leu 1 5 10 15 Gly Lys Thr Ala Thr Asp Ser Asp Glu Arg Ile Asp Asp Glu Ile 20 25 30 Asp Thr Glu Val Glu Glu Thr Gln Glu Glu Lys Ile Lys Leu Glu 35 40 45 Cys Glu Gln Ile Pro Lys Lys Phe Arg His Ser Ala Ile Ser Pro 50 55 60 Lys Ser Ser Leu His Arg Lys Ser Arg Ser Lys Asp Tyr Asp Val 65 70 75 Tyr Ser Asp Asn Asp Ile Cys Ser Gln Glu Ser Glu Asp Asn Phe 80 85 90 Ala Lys Glu Leu Gln Gln Tyr Ile Gln Ala Arg Glu Met Ala Asn 95 100 105 Ala Ala Gln Pro Glu Glu Ser Thr Lys Lys Glu Gly Val Lys Asp 110 115 120 Thr Pro Gln Ala Ala Lys Gln Lys Asn Lys Asn Leu Lys Ala Gly 125 130 135 His Lys Asn Gly Lys Gln Lys Lys Met Lys Arg Lys Trp Pro Gly 140 145 150 Pro Gly Asn Lys Gly Ser Asn Ala Leu Leu Arg Asn Ser Gly Ser 155 160 165 Gln Glu Glu Asp Gly Lys Pro Lys Glu Lys Gln Gln His Leu Ser 170 175 180 Gln Ala Phe Ile Asn Gln His Thr Val Glu Arg Lys Gly Lys Gln 185 190 195 Ile Cys Lys Tyr Phe Leu Glu Arg Lys Cys Ile Lys Gly Asp Gln 200 205 210 Cys Lys Phe Asp His Asp Ala Glu Ile Glu Lys Lys Lys Glu Met 215 220 225 Cys Lys Phe Tyr Val Gln Gly Tyr Cys Thr Arg Gly Glu Asn Cys 230 235 240 Leu Tyr Leu His Asn Glu Tyr Pro Cys Lys Phe Tyr His Thr Gly 245 250 255 Thr Lys Cys Tyr Gln Gly Glu Tyr Cys Lys Phe Ser His Ala Pro 260 265 270 Leu Thr Pro Glu Thr Gln Glu Leu Leu Ala Lys Val Leu Asp Thr 275 280 285 Glu Lys Lys Ser Cys Lys 290 13 451 PRT Homo sapiens misc_feature Incyte ID No 2472784CD1 13 Met Ala Gly Ala Gly Pro Ala Pro Gly Leu Pro Gly Ala Gly Gly 1 5 10 15 Pro Val Val Pro Gly Pro Gly Ala Gly Ile Pro Gly Lys Ser Gly 20 25 30 Glu Glu Arg Leu Lys Glu Met Glu Ala Glu Met Ala Leu Phe Glu 35 40 45 Gln Glu Val Leu Gly Ala Pro Val Pro Gly Ile Pro Thr Ala Val 50 55 60 Pro Ala Val Pro Thr Val Pro Thr Val Pro Thr Val Glu Ala Met 65 70 75 Gln Val Pro Ala Ala Pro Val Ile Arg Pro Ile Ile Ala Thr Asn 80 85 90 Thr Tyr Gln Gln Val Gln Gln Thr Leu Glu Ala Arg Ala Ala Ala 95 100 105 Ala Ala Thr Val Val Pro Pro Met Val Gly Gly Pro Pro Phe Val 110 115 120 Gly Pro Val Gly Phe Gly Pro Gly Asp Arg Ser His Leu Asp Ser 125 130 135 Pro Glu Ala Arg Glu Ala Met Phe Leu Arg Arg Ala Ala Ala Val 140 145 150 Pro Arg Pro Met Ala Leu Pro Pro Pro His Gln Ala Leu Val Gly 155 160 165 Pro Pro Leu Pro Gly Pro Pro Gly Pro Pro Met Met Leu Pro Pro 170 175 180 Met Ala Arg Ala Pro Gly Pro Pro Leu Gly Ser Met Ala Ala Leu 185 190 195 Arg Pro Pro Leu Glu Glu Pro Ala Ala Pro Arg Glu Leu Gly Leu 200 205 210 Gly Leu Gly Leu Gly Leu Lys Glu Lys Glu Glu Ala Val Val Ala 215 220 225 Ala Ala Ala Gly Leu Glu Glu Ala Ser Ala Ala Val Ala Val Gly 230 235 240 Ala Gly Gly Ala Pro Ala Gly Pro Ala Val Ile Gly Pro Ser Leu 245 250 255 Pro Leu Ala Leu Ala Met Pro Leu Pro Glu Pro Glu Pro Leu Pro 260 265 270 Leu Pro Leu Glu Val Val Arg Gly Leu Leu Pro Pro Leu Arg Ile 275 280 285 Pro Glu Leu Leu Ser Leu Arg Pro Arg Pro Arg Pro Pro Arg Pro 290 295 300 Glu Pro Pro Pro Gly Leu Met Ala Leu Glu Val Pro Glu Pro Leu 305 310 315 Gly Glu Asp Lys Lys Lys Gly Lys Pro Glu Lys Leu Lys Arg Cys 320 325 330 Ile Arg Thr Ala Ala Gly Ser Ser Trp Glu Asp Pro Ser Leu Leu 335 340 345 Glu Trp Asp Ala Asp Asp Phe Arg Ile Phe Cys Gly Asp Leu Gly 350 355 360 Asn Glu Val Asn Asp Asp Ile Leu Ala Arg Ala Phe Ser Arg Phe 365 370 375 Pro Ser Phe Leu Lys Ala Lys Val Ile Arg Asp Lys Arg Thr Gly 380 385 390 Lys Thr Lys Gly Tyr Gly Phe Val Ser Phe Lys Asp Pro Ser Asp 395 400 405 Tyr Val Arg Ala Met Arg Glu Met Asn Gly Lys Tyr Val Gly Ser 410 415 420 Arg Pro Ile Lys Leu Arg Lys Ser Met Trp Lys Asp Arg Asn Leu 425 430 435 Asp Val Val Arg Lys Lys Gln Lys Glu Lys Lys Lys Leu Gly Leu 440 445 450 Arg 14 600 PRT Homo sapiens misc_feature Incyte ID No 2598981CD1 14 Met Pro Glu Ile Arg Val Thr Pro Leu Gly Ala Gly Gln Asp Val 1 5 10 15 Gly Arg Ser Cys Ile Leu Val Ser Ile Ala Gly Lys Asn Val Met 20 25 30 Leu Asp Cys Gly Met His Met Gly Phe Asn Asp Asp Arg Arg Phe 35 40 45 Pro Asp Phe Ser Tyr Ile Thr Gln Asn Gly Arg Leu Thr Asp Phe 50 55 60 Leu Asp Cys Val Ile Ile Ser His Phe His Leu Asp His Cys Gly 65 70 75 Ala Leu Pro Tyr Phe Ser Glu Met Val Gly Tyr Asp Gly Pro Ile 80 85 90 Tyr Met Thr His Pro Thr Gln Ala Ile Cys Pro Ile Leu Leu Glu 95 100 105 Asp Tyr Arg Lys Ile Ala Val Asp Lys Lys Gly Glu Ala Asn Phe 110 115 120 Phe Thr Ser Gln Met Ile Lys Asp Cys Met Lys Lys Val Val Ala 125 130 135 Val His Leu His Gln Thr Val Gln Val Asp Asp Glu Leu Glu Ile 140 145 150 Lys Ala Tyr Tyr Ala Gly His Val Leu Gly Ala Ala Met Phe Gln 155 160 165 Ile Lys Val Gly Ser Glu Ser Val Val Tyr Thr Gly Asp Tyr Asn 170 175 180 Met Thr Pro Asp Arg His Leu Gly Ala Ala Trp Ile Asp Lys Cys 185 190 195 Arg Pro Asn Leu Leu Ile Thr Glu Ser Thr Tyr Ala Thr Thr Ile 200 205 210 Arg Asp Ser Lys Arg Cys Arg Glu Arg Asp Phe Leu Lys Lys Val 215 220 225 His Glu Thr Val Glu Arg Gly Gly Lys Val Leu Ile Pro Val Phe 230 235 240 Ala Leu Gly Arg Ala Gln Glu Leu Cys Ile Leu Leu Glu Thr Phe 245 250 255 Trp Glu Arg Met Asn Leu Lys Val Pro Ile Tyr Phe Ser Thr Gly 260 265 270 Leu Thr Glu Lys Ala Asn His Tyr Tyr Lys Leu Phe Ile Pro Trp 275 280 285 Thr Asn Gln Lys Ile Arg Lys Thr Phe Val Gln Arg Asn Met Phe 290 295 300 Glu Phe Lys His Ile Lys Ala Phe Asp Arg Ala Phe Ala Asp Asn 305 310 315 Pro Gly Pro Met Val Val Phe Ala Thr Pro Gly Met Leu His Ala 320 325 330 Gly Gln Ser Leu Gln Ile Phe Arg Lys Trp Ala Gly Asn Glu Lys 335 340 345 Asn Met Val Ile Met Pro Gly Tyr Cys Val Gln Gly Thr Val Gly 350 355 360 His Lys Ile Leu Ser Gly Gln Arg Lys Leu Glu Met Glu Gly Arg 365 370 375 Gln Val Leu Glu Val Lys Met Gln Val Glu Tyr Met Ser Phe Ser 380 385 390 Ala His Ala Asp Ala Lys Gly Ile Met Gln Leu Val Gly Gln Ala 395 400 405 Glu Pro Glu Ser Val Leu Leu Val His Gly Glu Ala Lys Lys Met 410 415 420 Glu Phe Leu Lys Gln Lys Ile Glu Gln Glu Leu Arg Val Asn Cys 425 430 435 Tyr Met Pro Ala Asn Gly Glu Thr Val Thr Leu Pro Thr Ser Pro 440 445 450 Ser Ile Pro Val Gly Ile Ser Leu Gly Leu Leu Lys Arg Glu Met 455 460 465 Ala Gln Gly Leu Leu Pro Glu Ala Lys Lys Pro Arg Leu Leu His 470 475 480 Gly Thr Leu Ile Met Lys Asp Ser Asn Phe Arg Leu Val Ser Ser 485 490 495 Glu Gln Ala Leu Lys Glu Leu Gly Leu Ala Glu His Gln Leu Arg 500 505 510 Phe Thr Cys Arg Val His Leu His Asp Thr Arg Lys Glu Gln Glu 515 520 525 Thr Ala Leu Arg Val Tyr Ser His Leu Lys Ser Val Leu Lys Asp 530 535 540 His Cys Val Gln His Leu Pro Asp Gly Ser Val Thr Val Glu Ser 545 550 555 Val Leu Leu Gln Ala Ala Ala Pro Ser Glu Asp Pro Gly Thr Lys 560 565 570 Val Leu Leu Val Ser Trp Thr Tyr Gln Asp Glu Glu Leu Gly Ser 575 580 585 Phe Leu Thr Ser Leu Leu Lys Lys Gly Leu Pro Gln Ala Pro Ser 590 595 600 15 217 PRT Homo sapiens misc_feature Incyte ID No 2738075CD1 15 Met Ser Gly Gly Leu Ala Pro Ser Lys Ser Thr Val Tyr Val Ser 1 5 10 15 Asn Leu Pro Phe Ser Leu Thr Asn Asn Asp Leu Tyr Arg Ile Phe 20 25 30 Ser Lys Tyr Gly Lys Val Val Lys Val Thr Ile Met Lys Asp Lys 35 40 45 Asp Thr Arg Lys Ser Lys Gly Val Ala Phe Ile Leu Phe Leu Asp 50 55 60 Lys Asp Ser Ala Gln Asn Cys Thr Arg Ala Ile Asn Asn Lys Gln 65 70 75 Leu Phe Gly Arg Val Ile Lys Ala Ser Ile Ala Ile Asp Asn Gly 80 85 90 Arg Ala Ala Glu Phe Ile Arg Arg Arg Asn Tyr Phe Asp Lys Ser 95 100 105 Lys Cys Tyr Glu Cys Gly Glu Ser Gly His Leu Ser Tyr Ala Cys 110 115 120 Pro Lys Asn Met Leu Gly Glu Arg Glu Pro Pro Lys Lys Lys Glu 125 130 135 Lys Lys Lys Lys Lys Lys Ala Pro Glu Pro Glu Glu Glu Ile Glu 140 145 150 Glu Val Glu Glu Ser Glu Asp Glu Gly Glu Asp Pro Ala Leu Asp 155 160 165 Ser Leu Ser Gln Ala Ile Ala Phe Gln Gln Ala Lys Ile Glu Glu 170 175 180 Glu Gln Lys Lys Trp Lys Pro Ser Ser Gly Val Pro Ser Thr Ser 185 190 195 Asp Asp Ser Arg Arg Pro Arg Ile Lys Lys Ser Thr Tyr Phe Ser 200 205 210 Asp Glu Glu Glu Leu Ser Asp 215 16 319 PRT Homo sapiens misc_feature Incyte ID No 2279049CD1 16 Met Lys Ile Glu Leu Ser Met Gln Pro Trp Asn Pro Gly Tyr Ser 1 5 10 15 Ser Glu Gly Ala Thr Ala Gln Glu Thr Tyr Thr Cys Pro Lys Met 20 25 30 Ile Glu Met Glu Gln Ala Glu Ala Gln Leu Ala Glu Leu Asp Leu 35 40 45 Leu Ala Ser Met Phe Pro Gly Glu Asn Glu Leu Ile Val Asn Asp 50 55 60 Gln Leu Ala Val Ala Glu Leu Lys Asp Cys Ile Glu Lys Lys Thr 65 70 75 Met Glu Gly Arg Ser Ser Lys Val Tyr Phe Thr Ile Asn Met Asn 80 85 90 Leu Asp Val Ser Asp Glu Lys Met Ala Met Phe Ser Leu Ala Cys 95 100 105 Ile Leu Pro Phe Lys Tyr Pro Ala Val Leu Pro Glu Ile Thr Val 110 115 120 Arg Ser Val Leu Leu Ser Arg Ser Gln Gln Thr Gln Leu Asn Thr 125 130 135 Asp Leu Thr Ala Phe Leu Gln Lys His Cys His Gly Asp Val Cys 140 145 150 Ile Leu Asn Ala Thr Glu Trp Val Arg Glu His Ala Ser Gly Tyr 155 160 165 Val Ser Arg Asp Thr Ser Ser Ser Pro Thr Thr Gly Ser Thr Val 170 175 180 Gln Ser Val Asp Leu Ile Phe Thr Arg Leu Trp Ile Tyr Ser His 185 190 195 His Ile Tyr Asn Lys Cys Lys Arg Lys Asn Ile Leu Glu Trp Ala 200 205 210 Lys Glu Leu Ser Leu Ser Gly Phe Ser Met Pro Gly Lys Pro Gly 215 220 225 Val Val Cys Val Glu Gly Pro Gln Ser Ala Cys Glu Glu Phe Trp 230 235 240 Ser Arg Leu Arg Lys Leu Asn Trp Lys Arg Ile Leu Ile Arg His 245 250 255 Arg Glu Asp Ile Pro Phe Asp Gly Thr Asn Asp Glu Thr Glu Arg 260 265 270 Gln Arg Lys Phe Ser Ile Phe Glu Glu Lys Val Phe Ser Val Asn 275 280 285 Gly Ala Arg Gly Asn His Met Asp Phe Gly Gln Leu Tyr Gln Phe 290 295 300 Leu Asn Thr Lys Gly Cys Gly Asp Val Phe Gln Met Phe Phe Gly 305 310 315 Val Glu Gly Gln 17 108 PRT Homo sapiens misc_feature Incyte ID No 2660904CD1 17 Met Ser His His Ala Glu Ile Gln Arg Asp Ile Leu Glu Ser Cys 1 5 10 15 Asn His Val Arg Lys Lys Val Pro Val Thr Phe Val Gly Ala Gly 20 25 30 Gly Gln Asp Pro Glu Val Pro Glu Glu Leu Leu His Leu Leu Gln 35 40 45 Pro Gly Gln Arg Val Pro Gln Asp Val Gln His His Leu Leu Glu 50 55 60 Pro Arg Asp Arg Trp Ala His Leu Glu Val Leu Lys Lys Val Asp 65 70 75 Leu Leu Leu Gln Val Met Ala Ala Thr Gly Tyr Phe His Ala Ser 80 85 90 Leu Gln Arg Gly Glu Ile Met Arg Ser Pro Gly Pro Val Ala Arg 95 100 105 Asn Ser Pro 18 92 PRT Homo sapiens misc_feature Incyte ID No 3179424CD1 18 Met Ala Val Leu Ala Gly Ser Leu Leu Gly Pro Thr Ser Arg Ser 1 5 10 15 Ala Ala Leu Leu Gly Gly Arg Trp Leu Gln Pro Arg Ala Trp Leu 20 25 30 Gly Phe Pro Asp Ala Trp Gly Leu Pro Thr Pro Gln Gln Ala Arg 35 40 45 Gly Lys Ala Arg Gly Asn Glu Tyr Gln Pro Ser Asn Ile Lys Arg 50 55 60 Lys Asn Lys His Gly Trp Val Arg Arg Leu Ser Thr Pro Ala Gly 65 70 75 Val Gln Val Ile Leu Arg Arg Met Leu Lys Gly Arg Lys Ser Leu 80 85 90 Ser His 19 268 PRT Homo sapiens misc_feature Incyte ID No 2885096CD1 19 Met Ala Gly Gly Val Pro Gly Gln Pro Ala Gly Val Gly Leu Ala 1 5 10 15 Leu Ile Ala Thr Asp Ser Gln Glu Thr Arg Pro Gly Arg Ala Gly 20 25 30 Pro Gly Ser Gly Glu Ser Leu Ser Ala Ser His Leu Phe Ile Ser 35 40 45 Asp Phe Ala Tyr Cys Trp Glu Asn Phe Val Cys Asn Glu Gly Gln 50 55 60 Pro Phe Met Pro Trp Tyr Lys Phe Asp Asp Asn Tyr Ala Ser Leu 65 70 75 His Arg Thr Leu Lys Glu Ile Leu Arg Asn Pro Met Glu Ala Met 80 85 90 Tyr Pro His Ile Phe Tyr Phe His Phe Lys Asn Leu Leu Lys Ala 95 100 105 Cys Gly Arg Asn Glu Ser Trp Leu Cys Phe Thr Met Glu Val Thr 110 115 120 Lys His His Ser Ala Val Phe Arg Lys Lys Gly Val Phe Arg Asn 125 130 135 Gln Val Asp Pro Glu Thr His Cys His Ala Glu Arg Cys Phe Leu 140 145 150 Ser Trp Phe Cys Asp Asp Ile Leu Ser Pro Asn Thr Asn Tyr Glu 155 160 165 Val Thr Trp Tyr Thr Ser Trp Ser Pro Cys Pro Glu Cys Ala Gly 170 175 180 Glu Val Ala Glu Phe Leu Ala Arg His Ser Asn Val Asn Leu Thr 185 190 195 Ile Phe Thr Ala Arg Leu Cys Tyr Phe Trp Asp Thr Asp Tyr Gln 200 205 210 Glu Gly Leu Cys Ser Leu Ser Gln Glu Gly Ala Ser Val Lys Ile 215 220 225 Met Gly Tyr Lys Asp Phe Val Ser Cys Trp Lys Asn Phe Val Tyr 230 235 240 Ser Asp Asp Glu Pro Phe Lys Pro Trp Lys Gly Leu Gln Thr Asn 245 250 255 Phe Arg Leu Leu Lys Arg Arg Leu Arg Glu Ile Leu Gln 260 265 20 624 PRT Homo sapiens misc_feature Incyte ID No 2901076CD1 20 Met Asn Ser Gly Gly Gly Phe Gly Leu Gly Leu Gly Phe Gly Leu 1 5 10 15 Thr Pro Thr Ser Val Ile Gln Val Thr Asn Leu Ser Ser Ala Val 20 25 30 Thr Ser Glu Gln Met Arg Thr Leu Phe Ser Phe Leu Gly Glu Ile 35 40 45 Glu Glu Leu Arg Leu Tyr Pro Pro Asp Asn Ala Pro Leu Ala Phe 50 55 60 Ser Ser Lys Val Cys Tyr Val Lys Phe Arg Asp Pro Ser Ser Val 65 70 75 Gly Val Ala Gln His Leu Thr Asn Thr Val Phe Ile Asp Arg Ala 80 85 90 Leu Ile Val Val Pro Cys Ala Glu Gly Lys Ile Pro Glu Glu Ser 95 100 105 Lys Ala Leu Ser Leu Leu Ala Pro Ala Pro Thr Met Thr Ser Leu 110 115 120 Met Pro Gly Ala Gly Leu Leu Pro Ile Pro Thr Pro Asn Pro Leu 125 130 135 Thr Thr Leu Gly Val Ser Leu Ser Ser Leu Gly Ala Ile Pro Ala 140 145 150 Ala Ala Leu Asp Pro Asn Ile Ala Thr Leu Gly Glu Ile Pro Gln 155 160 165 Pro Pro Leu Met Gly Asn Val Asp Pro Ser Lys Ile Asp Glu Ile 170 175 180 Arg Arg Thr Val Tyr Val Gly Asn Leu Asn Ser Gln Thr Thr Thr 185 190 195 Ala Asp Gln Leu Leu Glu Phe Phe Lys Gln Val Gly Glu Val Lys 200 205 210 Phe Val Arg Met Ala Gly Asp Glu Thr Gln Pro Thr Arg Phe Ala 215 220 225 Phe Val Glu Phe Ala Asp Gln Asn Ser Val Pro Arg Ala Leu Ala 230 235 240 Phe Asn Gly Val Met Phe Gly Asp Arg Pro Leu Lys Ile Asn His 245 250 255 Ser Asn Asn Ala Ile Val Lys Pro Pro Glu Met Thr Pro Gln Ala 260 265 270 Ala Ala Lys Glu Leu Glu Glu Val Met Lys Arg Val Arg Glu Ala 275 280 285 Gln Ser Phe Ile Ser Ala Ala Ile Glu Pro Glu Ser Gly Lys Ser 290 295 300 Asn Glu Arg Lys Gly Gly Arg Ser Arg Ser His Thr Arg Ser Lys 305 310 315 Ser Arg Ser Ser Ser Lys Ser His Ser Arg Arg Lys Arg Ser Gln 320 325 330 Ser Lys His Arg Ser Arg Ser His Asn Arg Ser Arg Ser Arg Gln 335 340 345 Lys Asp Arg Arg Arg Ser Lys Ser Pro His Lys Lys Arg Ser Lys 350 355 360 Ser Arg Glu Arg Arg Lys Ser Arg Ser Arg Ser His Ser Arg Asp 365 370 375 Lys Arg Lys Asp Thr Arg Glu Lys Ile Lys Glu Lys Glu Arg Val 380 385 390 Lys Glu Lys Asp Arg Glu Lys Glu Arg Glu Arg Glu Lys Glu Arg 395 400 405 Glu Lys Glu Lys Glu Arg Gly Lys Asn Lys Asp Arg Asp Lys Glu 410 415 420 Arg Glu Lys Asp Arg Glu Lys Asp Lys Glu Lys Asp Arg Glu Arg 425 430 435 Glu Arg Glu Lys Glu His Glu Lys Asp Arg Asp Lys Glu Lys Glu 440 445 450 Lys Glu Gln Asp Lys Glu Lys Glu Arg Glu Lys Asp Arg Ser Lys 455 460 465 Glu Ile Asp Glu Lys Arg Lys Lys Asp Lys Lys Ser Arg Thr Pro 470 475 480 Pro Arg Ser Tyr Asn Ala Ser Arg Arg Ser Arg Ser Ser Ser Arg 485 490 495 Glu Arg Arg Arg Arg Arg Ser Arg Ser Ser Ser Arg Ser Pro Arg 500 505 510 Thr Ser Lys Thr Ile Lys Arg Lys Ser Ser Arg Ser Pro Ser Pro 515 520 525 Arg Ser Arg Asn Lys Lys Asp Lys Lys Arg Glu Lys Glu Arg Asp 530 535 540 His Ile Ser Glu Arg Arg Glu Arg Glu Arg Ser Thr Ser Met Arg 545 550 555 Lys Ser Ser Asn Asp Arg Asp Gly Lys Glu Lys Leu Glu Lys Asn 560 565 570 Ser Thr Ser Leu Lys Glu Lys Glu His Asn Lys Glu Pro Asp Ser 575 580 585 Ser Val Ser Lys Glu Val Asp Asp Lys Asp Ala Pro Arg Thr Glu 590 595 600 Glu Asn Lys Ile Gln His Asn Gly Asn Cys Gln Leu Asn Glu Glu 605 610 615 Asn Leu Ser Thr Lys Thr Glu Ala Val 620 21 419 PRT Homo sapiens misc_feature Incyte ID No 3074572CD1 21 Met Ala Ala Glu Val Leu Pro Ser Ala Arg Trp Gln Tyr Cys Gly 1 5 10 15 Ala Pro Asp Gly Ser Gln Arg Ala Val Leu Val Gln Phe Ser Asn 20 25 30 Gly Lys Leu Gln Ser Pro Gly Asn Met Arg Phe Thr Leu Tyr Glu 35 40 45 Asn Lys Asp Ser Thr Asn Pro Arg Lys Arg Asn Gln Arg Ile Leu 50 55 60 Ala Ala Glu Thr Asp Arg Leu Ser Tyr Val Gly Asn Asn Phe Gly 65 70 75 Thr Gly Ala Leu Lys Cys Asn Thr Leu Cys Arg His Phe Val Gly 80 85 90 Ile Leu Asn Lys Thr Ser Gly Gln Met Glu Val Tyr Asp Ala Glu 95 100 105 Leu Phe Asn Met Gln Pro Leu Phe Ser Asp Val Ser Val Glu Ser 110 115 120 Glu Leu Ala Leu Glu Ser Gln Thr Lys Thr Tyr Arg Glu Lys Met 125 130 135 Asp Ser Cys Ile Glu Ala Phe Gly Thr Thr Lys Gln Lys Arg Ala 140 145 150 Leu Asn Thr Arg Arg Met Asn Arg Val Gly Asn Glu Ser Leu Asn 155 160 165 Arg Ala Val Ala Lys Ala Ala Glu Thr Ile Ile Asp Thr Lys Gly 170 175 180 Val Thr Ala Leu Val Ser Asp Ala Ile His Asn Asp Leu Gln Asp 185 190 195 Asp Ser Leu Tyr Leu Pro Pro Cys Tyr Asp Asp Ala Ala Lys Pro 200 205 210 Glu Asp Val Tyr Lys Phe Glu Asp Leu Leu Ser Pro Ala Glu Tyr 215 220 225 Glu Ala Leu Gln Ser Pro Ser Glu Ala Phe Arg Asn Val Thr Ser 230 235 240 Glu Glu Ile Leu Lys Met Ile Glu Glu Asn Ser His Cys Thr Phe 245 250 255 Val Ile Glu Ala Leu Lys Ser Leu Pro Ser Asp Val Glu Ser Arg 260 265 270 Asp Arg Gln Ala Arg Cys Ile Trp Phe Leu Asp Thr Leu Ile Lys 275 280 285 Phe Arg Ala His Arg Val Val Lys Arg Lys Ser Ala Leu Gly Pro 290 295 300 Gly Val Pro His Ile Ile Asn Thr Lys Leu Leu Lys His Phe Thr 305 310 315 Cys Leu Thr Tyr Asn Asn Gly Arg Leu Arg Asn Leu Ile Ser Asp 320 325 330 Ser Met Lys Ala Lys Ile Thr Ala Tyr Val Ile Ile Leu Ala Leu 335 340 345 His Ile His Asp Phe Gln Ile Asp Leu Thr Val Leu Gln Arg Asp 350 355 360 Leu Lys Leu Ser Glu Lys Arg Met Met Glu Ile Ala Lys Ala Met 365 370 375 Arg Leu Lys Ile Ser Lys Arg Arg Val Ser Val Ala Ala Gly Ser 380 385 390 Glu Glu Asp His Lys Leu Gly Thr Leu Ser Leu Pro Leu Pro Pro 395 400 405 Ala Gln Thr Ser Asp Arg Leu Ala Lys Arg Arg Lys Ile Thr 410 415 22 743 PRT Homo sapiens misc_feature Incyte ID No 1437895CD1 22 Met Glu Glu Glu Gly Leu Glu Cys Pro Asn Ser Ser Ser Glu Lys 1 5 10 15 Arg Tyr Phe Pro Glu Ser Leu Asp Ser Ser Asp Gly Asp Glu Glu 20 25 30 Glu Val Leu Ala Cys Glu Asp Leu Glu Leu Asn Pro Phe Asp Gly 35 40 45 Leu Pro Tyr Ser Ser Arg Tyr Tyr Lys Leu Leu Lys Glu Arg Glu 50 55 60 Asp Leu Pro Ile Trp Lys Glu Lys Tyr Ser Phe Met Glu Asn Leu 65 70 75 Leu Gln Asn Gln Ile Val Ile Val Ser Gly Asp Ala Lys Cys Gly 80 85 90 Lys Ser Ala Gln Val Pro Gln Trp Cys Ala Glu Tyr Cys Leu Ser 95 100 105 Ile His Tyr Gln His Gly Gly Val Ile Cys Thr Gln Val His Lys 110 115 120 Gln Thr Val Val Gln Leu Ala Leu Arg Val Ala Asp Glu Met Asp 125 130 135 Val Asn Ile Gly His Glu Val Gly Tyr Val Ile Pro Phe Glu Asn 140 145 150 Cys Cys Thr Asn Glu Thr Ile Leu Arg Tyr Cys Thr Asp Asp Met 155 160 165 Leu Gln Arg Glu Met Met Ser Asn Pro Phe Leu Gly Ser Tyr Gly 170 175 180 Val Ile Ile Leu Asp Asp Ile His Glu Arg Ser Ile Ala Thr Asp 185 190 195 Val Leu Leu Gly Leu Leu Lys Asp Val Leu Leu Ala Arg Pro Glu 200 205 210 Leu Lys Leu Ile Ile Asn Ser Ser Pro His Leu Ile Ser Lys Leu 215 220 225 Asn Ser Tyr Tyr Gly Asn Val Pro Val Ile Glu Val Lys Asn Lys 230 235 240 His Pro Val Glu Val Val Tyr Leu Ser Glu Ala Gln Lys Asp Ser 245 250 255 Phe Glu Ser Ile Leu Arg Leu Ile Phe Glu Ile His His Ser Gly 260 265 270 Glu Lys Gly Asp Ile Val Val Phe Leu Ala Cys Glu Gln Asp Ile 275 280 285 Glu Lys Val Cys Glu Thr Val Tyr Gln Gly Ser Asn Leu Asn Pro 290 295 300 Asp Leu Gly Glu Leu Val Val Val Pro Leu Tyr Pro Lys Glu Lys 305 310 315 Cys Ser Leu Phe Lys Pro Leu Asp Glu Thr Glu Lys Arg Cys Gln 320 325 330 Val Tyr Gln Arg Arg Val Val Leu Thr Thr Ser Ser Gly Glu Phe 335 340 345 Leu Ile Trp Ser Asn Ser Val Arg Phe Val Ile Asp Val Gly Val 350 355 360 Glu Arg Arg Lys Val Tyr Asn Pro Arg Ile Arg Ala Asn Ser Leu 365 370 375 Val Met Gln Pro Ile Ser Gln Ser Gln Ala Glu Ile Arg Lys Gln 380 385 390 Ile Leu Gly Ser Ser Ser Ser Gly Lys Phe Phe Cys Leu Tyr Thr 395 400 405 Glu Glu Phe Ala Ser Lys Asp Met Thr Pro Leu Lys Pro Ala Glu 410 415 420 Met Gln Glu Ala Asn Leu Thr Ser Met Val Leu Phe Met Lys Arg 425 430 435 Ile Asp Ile Ala Gly Leu Gly His Cys Asp Phe Met Asn Arg Pro 440 445 450 Ala Pro Glu Ser Leu Met Gln Ala Leu Glu Asp Leu Asp Tyr Leu 455 460 465 Ala Ala Leu Asp Asn Asp Gly Asn Leu Ser Glu Phe Gly Ile Ile 470 475 480 Met Ser Glu Phe Pro Leu Asp Pro Gln Leu Ser Lys Ser Ile Leu 485 490 495 Ala Ser Cys Glu Phe Asp Cys Val Asp Glu Val Leu Thr Ile Ala 500 505 510 Ala Met Val Thr Ala Pro Asn Cys Phe Ser His Val Pro His Gly 515 520 525 Ala Glu Glu Ala Ala Leu Thr Cys Trp Lys Thr Phe Leu His Pro 530 535 540 Glu Gly Asp His Phe Thr Leu Ile Ser Ile Tyr Lys Ala Tyr Gln 545 550 555 Asp Thr Thr Leu Asn Ser Ser Ser Glu Tyr Cys Val Glu Lys Trp 560 565 570 Cys Arg Asp Tyr Phe Leu Asn Cys Ser Ala Leu Arg Met Ala Asp 575 580 585 Val Ile Arg Ala Glu Leu Leu Glu Ile Ile Lys Arg Ile Glu Leu 590 595 600 Pro Tyr Ala Glu Pro Ala Phe Gly Ser Lys Glu Asn Thr Leu Asn 605 610 615 Ile Lys Lys Ala Leu Leu Ser Gly Tyr Phe Met Gln Ile Ala Arg 620 625 630 Asp Val Asp Gly Ser Gly Asn Tyr Leu Met Leu Thr His Lys Gln 635 640 645 Val Ala Gln Leu His Pro Leu Ser Gly Tyr Ser Ile Thr Lys Lys 650 655 660 Met Pro Glu Trp Val Leu Phe His Lys Phe Ser Ile Ser Glu Asn 665 670 675 Asn Tyr Ile Arg Ile Thr Ser Glu Ile Ser Pro Glu Leu Phe Met 680 685 690 Gln Leu Val Pro Gln Tyr Tyr Phe Ser Asn Leu Pro Pro Ser Glu 695 700 705 Ser Lys Asp Ile Leu Gln Gln Val Val Asp His Leu Ser Pro Val 710 715 720 Ser Thr Met Asn Lys Glu Gln Gln Met Cys Glu Thr Cys Pro Glu 725 730 735 Thr Glu Gln Arg Cys Thr Leu Gln 740 23 284 PRT Homo sapiens misc_feature Incyte ID No 1454656CD1 23 Met Arg Arg Pro Cys Asn Pro Val Arg Ala Ala Lys Arg Thr Ala 1 5 10 15 Ala Ala Ala Arg Ala Pro Arg Gly Leu Glu Val Thr Met Leu Arg 20 25 30 Val Ala Trp Arg Thr Leu Ser Leu Ile Arg Thr Arg Ala Val Thr 35 40 45 Gln Val Leu Val Pro Gly Leu Pro Gly Gly Gly Ser Ala Lys Phe 50 55 60 Pro Phe Asn Gln Trp Gly Leu Gln Pro Arg Ser Leu Leu Leu Gln 65 70 75 Ala Ala Arg Gly Tyr Val Val Arg Lys Pro Ala Gln Ser Arg Leu 80 85 90 Asp Asp Asp Pro Pro Pro Ser Thr Leu Leu Lys Asp Tyr Gln Asn 95 100 105 Val Pro Gly Ile Glu Lys Val Asp Asp Val Val Lys Arg Leu Leu 110 115 120 Ser Leu Glu Met Ala Asn Lys Lys Glu Met Leu Lys Ile Lys Gln 125 130 135 Glu Gln Phe Met Lys Lys Ile Val Ala Asn Pro Glu Asp Thr Arg 140 145 150 Ser Leu Glu Ala Arg Ile Ile Ala Leu Ser Val Lys Ile Arg Ser 155 160 165 Tyr Glu Glu His Leu Glu Lys His Arg Lys Asp Lys Ala His Lys 170 175 180 Arg Tyr Leu Leu Met Ser Ile Asp Gln Arg Lys Lys Met Leu Lys 185 190 195 Asn Leu Arg Asn Thr Asn Tyr Asp Val Phe Glu Lys Ile Cys Trp 200 205 210 Gly Leu Gly Ile Glu Tyr Thr Phe Pro Pro Leu Tyr Tyr Arg Arg 215 220 225 Ala His Arg Arg Phe Val Thr Lys Lys Ala Leu Cys Ile Arg Val 230 235 240 Phe Gln Glu Thr Gln Lys Leu Lys Lys Arg Arg Arg Ala Leu Lys 245 250 255 Ala Ala Ala Ala Ala Gln Lys Gln Ala Lys Arg Arg Asn Pro Asp 260 265 270 Ser Pro Ala Lys Ala Ile Pro Lys Thr Leu Lys Asp Ser Gln 275 280 24 248 PRT Homo sapiens misc_feature Incyte ID No 121130CD1 24 Met Ala Ala Gln Ser Ala Pro Lys Val Val Leu Lys Ser Thr Thr 1 5 10 15 Lys Met Ser Leu Asn Glu Arg Phe Thr Asn Met Leu Lys Asn Lys 20 25 30 Gln Pro Thr Pro Val Asn Ile Arg Ala Ser Met Gln Gln Gln Gln 35 40 45 Gln Leu Ala Ser Ala Arg Asn Arg Arg Leu Ala Gln Gln Met Glu 50 55 60 Asn Arg Pro Ser Val Gln Ala Ala Leu Lys Leu Lys Gln Ser Leu 65 70 75 Lys Gln Arg Leu Gly Lys Ser Asn Ile Gln Ala Arg Leu Gly Arg 80 85 90 Pro Ile Gly Ala Leu Ala Arg Gly Ala Ile Gly Gly Arg Gly Leu 95 100 105 Pro Ile Ile Gln Arg Gly Leu Pro Arg Gly Gly Leu Arg Gly Gly 110 115 120 Arg Ala Thr Arg Thr Leu Leu Arg Gly Gly Met Ser Leu Arg Gly 125 130 135 Gln Asn Leu Leu Arg Gly Gly Arg Ala Val Ala Pro Arg Met Gly 140 145 150 Leu Arg Arg Gly Gly Val Arg Gly Arg Gly Gly Pro Gly Arg Gly 155 160 165 Gly Leu Gly Arg Gly Ala Met Gly Arg Gly Gly Ile Gly Gly Arg 170 175 180 Gly Arg Gly Met Ile Gly Arg Gly Arg Gly Gly Phe Gly Gly Arg 185 190 195 Gly Arg Gly Arg Gly Arg Gly Arg Gly Ala Leu Ala Arg Pro Val 200 205 210 Leu Thr Lys Glu Gln Leu Asp Asn Gln Leu Asp Ala Tyr Met Ser 215 220 225 Lys Thr Lys Gly His Leu Asp Ala Glu Leu Asp Ala Tyr Met Ala 230 235 240 Gln Thr Asp Pro Glu Thr Asn Asp 245 25 214 PRT Homo sapiens misc_feature Incyte ID No 1257715CD1 25 Met Arg Pro Gly Gly Phe Leu Gly Ala Gly Gln Arg Leu Ser Arg 1 5 10 15 Ala Met Ser Arg Cys Val Leu Glu Pro Arg Pro Pro Gly Lys Arg 20 25 30 Trp Met Val Ala Gly Leu Gly Asn Pro Gly Leu Pro Gly Thr Arg 35 40 45 His Ser Val Gly Met Ala Val Leu Gly Gln Leu Ala Arg Arg Leu 50 55 60 Gly Val Ala Glu Ser Trp Thr Arg Asp Arg His Cys Ala Ala Asp 65 70 75 Leu Ala Leu Ala Pro Leu Gly Asp Ala Gln Leu Val Leu Leu Arg 80 85 90 Pro Arg Arg Leu Met Asn Ala Asn Gly Arg Ser Val Ala Arg Ala 95 100 105 Ala Glu Leu Phe Gly Leu Thr Ala Glu Glu Val Tyr Leu Val His 110 115 120 Asp Glu Leu Asp Lys Pro Leu Gly Arg Leu Ala Leu Lys Leu Gly 125 130 135 Gly Ser Ala Arg Gly His Asn Gly Val Arg Ser Cys Ile Ser Cys 140 145 150 Leu Asn Ser Asn Ala Met Pro Arg Leu Arg Val Gly Ile Gly Arg 155 160 165 Pro Ala His Pro Glu Ala Val Gln Ala His Val Leu Gly Cys Phe 170 175 180 Ser Pro Ala Glu Gln Glu Leu Leu Pro Leu Leu Leu Asp Arg Ala 185 190 195 Thr Asp Leu Ile Leu Asp His Ile Arg Glu Arg Ser Gln Gly Pro 200 205 210 Ser Leu Gly Pro 26 184 PRT Homo sapiens misc_feature Incyte ID No 1342022CD1 26 Met Thr Thr Arg Pro Ala Phe Ile Leu His His Ser Asp Cys Phe 1 5 10 15 Ser Ser Arg Ser Ser Arg Ile Arg His Glu Gly Val Trp Arg Arg 20 25 30 Arg Ala Glu Met Ala Pro Arg Lys Gly Lys Glu Lys Lys Glu Glu 35 40 45 Gln Val Ile Ser Leu Gly Pro Gln Val Ala Glu Gly Glu Asn Val 50 55 60 Phe Gly Val Cys His Ile Phe Ala Ser Phe Asn Asp Thr Phe Val 65 70 75 His Val Thr Asp Leu Ser Gly Lys Glu Thr Ile Cys Arg Val Thr 80 85 90 Gly Gly Met Lys Val Lys Ala Asp Arg Asp Glu Ser Ser Pro Tyr 95 100 105 Ala Ala Met Leu Ala Ala Gln Asp Val Ala Gln Arg Cys Lys Glu 110 115 120 Leu Gly Ile Thr Ala Leu His Ile Lys Leu Arg Ala Thr Gly Gly 125 130 135 Asn Arg Thr Lys Thr Pro Gly Pro Gly Ala Gln Ser Ala Leu Arg 140 145 150 Ala Leu Ala Arg Ser Gly Met Lys Ile Gly Arg Ile Glu Asp Val 155 160 165 Thr Pro Ile Pro Ser Asp Ser Thr Arg Arg Lys Gly Gly Arg Arg 170 175 180 Gly Arg Arg Leu 27 371 PRT Homo sapiens misc_feature Incyte ID No 194704CD1 27 Met Ser Ala Gln Ala Gln Met Arg Ala Leu Leu Asp Gln Leu Met 1 5 10 15 Gly Thr Ala Arg Asp Gly Asp Glu Thr Arg Gln Arg Val Lys Phe 20 25 30 Thr Asp Asp Arg Val Cys Lys Ser His Leu Leu Asp Cys Cys Pro 35 40 45 His Asp Ile Leu Ala Gly Thr Arg Met Asp Leu Gly Glu Cys Thr 50 55 60 Lys Ile His Asp Leu Ala Leu Arg Ala Asp Tyr Glu Ile Ala Ser 65 70 75 Lys Glu Arg Asp Leu Phe Phe Glu Leu Asp Ala Met Asp His Leu 80 85 90 Glu Ser Phe Ile Ala Glu Cys Asp Arg Arg Thr Glu Leu Ala Lys 95 100 105 Lys Arg Leu Ala Glu Thr Gln Glu Glu Ile Ser Ala Glu Val Ser 110 115 120 Ala Lys Ala Glu Lys Val His Glu Leu Asn Glu Glu Ile Gly Lys 125 130 135 Leu Leu Ala Lys Ala Glu Gln Leu Gly Ala Glu Gly Asn Val Asp 140 145 150 Glu Ser Gln Lys Ile Leu Met Glu Val Glu Lys Val Arg Ala Lys 155 160 165 Lys Lys Glu Ala Glu Glu Glu Tyr Arg Asn Ser Met Pro Ala Ser 170 175 180 Ser Phe Gln Gln Gln Lys Leu Arg Val Cys Glu Val Cys Ser Ala 185 190 195 Tyr Leu Gly Leu His Asp Asn Asp Arg Arg Leu Ala Asp His Phe 200 205 210 Gly Gly Lys Leu His Leu Gly Phe Ile Gln Ile Arg Glu Lys Leu 215 220 225 Asp Gln Leu Arg Lys Thr Val Ala Glu Lys Gln Glu Lys Arg Asn 230 235 240 Gln Asp Arg Leu Arg Arg Arg Glu Glu Arg Glu Arg Glu Glu Arg 245 250 255 Leu Ser Arg Arg Ser Gly Ser Arg Thr Arg Asp Arg Arg Arg Ser 260 265 270 Arg Ser Arg Asp Arg Arg Arg Arg Arg Ser Arg Ser Thr Ser Arg 275 280 285 Glu Arg Arg Lys Leu Ser Arg Ser Arg Ser Arg Asp Arg His Arg 290 295 300 Arg His Arg Ser Arg Ser Arg Ser His Ser Arg Gly His Arg Arg 305 310 315 Ala Ser Arg Asp Arg Ser Ala Lys Tyr Lys Phe Ser Arg Glu Arg 320 325 330 Ala Ser Arg Glu Glu Ser Trp Glu Ser Gly Arg Ser Glu Arg Gly 335 340 345 Pro Pro Asp Trp Arg Leu Glu Ser Ser Asn Gly Lys Met Ala Ser 350 355 360 Arg Arg Ser Glu Glu Lys Glu Ala Gly Glu Ile 365 370 28 396 PRT Homo sapiens misc_feature Incyte ID No 607270CD1 28 Met Ala Ala Pro Cys Val Ser Tyr Gly Gly Ala Val Ser Tyr Arg 1 5 10 15 Leu Leu Leu Trp Gly Arg Gly Ser Leu Ala Arg Lys Gln Gly Leu 20 25 30 Trp Lys Thr Ala Ala Pro Glu Leu Gln Thr Asn Val Arg Ser Gln 35 40 45 Ile Leu Arg Leu Arg His Thr Ala Phe Val Ile Pro Lys Lys Asn 50 55 60 Val Pro Thr Ser Lys Arg Glu Thr Tyr Thr Glu Asp Phe Ile Lys 65 70 75 Lys Gln Ile Glu Glu Phe Asn Ile Gly Lys Arg His Leu Ala Asn 80 85 90 Met Met Gly Glu Asp Pro Glu Thr Phe Thr Gln Glu Asp Ile Asp 95 100 105 Arg Ala Ile Ala Tyr Leu Phe Pro Ser Gly Leu Phe Glu Lys Arg 110 115 120 Ala Arg Pro Val Met Lys His Pro Glu Gln Ile Phe Pro Arg Gln 125 130 135 Arg Ala Ile Gln Trp Gly Glu Asp Gly Arg Pro Phe His Tyr Leu 140 145 150 Phe Tyr Thr Gly Lys Gln Ser Tyr Tyr Ser Leu Met His Asp Val 155 160 165 Tyr Gly Met Leu Leu Asn Leu Glu Lys His Gln Ser His Leu Gln 170 175 180 Ala Lys Ser Leu Leu Pro Glu Lys Thr Val Thr Arg Asp Val Ile 185 190 195 Gly Ser Arg Trp Leu Ile Lys Glu Glu Leu Glu Glu Met Leu Val 200 205 210 Glu Lys Leu Ser Asp Leu Asp Tyr Met Gln Phe Ile Arg Leu Leu 215 220 225 Glu Lys Leu Leu Thr Ser Gln Cys Gly Ala Ala Glu Glu Glu Phe 230 235 240 Val Gln Arg Phe Arg Arg Ser Val Thr Leu Glu Ser Lys Lys Gln 245 250 255 Leu Ile Glu Pro Val Gln Tyr Asp Glu Gln Gly Met Ala Phe Ser 260 265 270 Lys Ser Glu Gly Lys Arg Lys Thr Ala Lys Ala Glu Ala Ile Val 275 280 285 Tyr Lys His Gly Ser Gly Arg Ile Lys Val Asn Gly Ile Asp Tyr 290 295 300 Gln Leu Tyr Phe Pro Ile Thr Gln Asp Arg Glu Gln Leu Met Phe 305 310 315 Pro Phe His Phe Val Asp Arg Leu Gly Lys His Asp Val Thr Cys 320 325 330 Thr Val Ser Gly Gly Gly Arg Ser Ala Gln Ala Gly Ala Ile Arg 335 340 345 Leu Ala Met Ala Lys Ala Leu Cys Ser Phe Val Thr Glu Asp Glu 350 355 360 Val Glu Trp Met Arg Gln Ala Gly Leu Leu Thr Thr Asp Pro Arg 365 370 375 Val Arg Glu Arg Lys Lys Pro Gly Gln Glu Gly Ala Arg Arg Lys 380 385 390 Phe Thr Trp Lys Lys Arg 395 29 184 PRT Homo sapiens misc_feature Incyte ID No 758546CD1 29 Met Val Arg Lys Leu Lys Phe His Glu Gln Lys Leu Leu Lys Gln 1 5 10 15 Val Asp Phe Leu Asn Trp Glu Val Thr Asp His Asn Leu His Glu 20 25 30 Leu Arg Val Leu Arg Arg Tyr Arg Leu Gln Arg Arg Glu Asp Tyr 35 40 45 Thr Arg Tyr Asn Gln Leu Ser Arg Ala Val Arg Glu Leu Ala Arg 50 55 60 Arg Leu Arg Asp Leu Pro Glu Arg Asp Gln Phe Arg Val Arg Ala 65 70 75 Ser Ala Ala Leu Leu Asp Lys Leu Tyr Ala Leu Gly Leu Val Pro 80 85 90 Thr Arg Gly Ser Leu Glu Leu Cys Asp Phe Val Thr Ala Ser Ser 95 100 105 Phe Cys Arg Arg Arg Leu Pro Thr Val Leu Leu Lys Leu Arg Met 110 115 120 Ala Gln His Leu Gln Ala Ala Val Ala Phe Val Glu Gln Gly His 125 130 135 Val Arg Val Gly Pro Asp Val Val Thr Asp Pro Ala Phe Leu Val 140 145 150 Thr Arg Ser Met Glu Asp Phe Val Thr Trp Val Asp Ser Ser Lys 155 160 165 Ile Lys Arg His Val Leu Glu Tyr Asn Glu Glu Arg Asp Asp Phe 170 175 180 Asp Leu Glu Ala 30 282 PRT Homo sapiens misc_feature Incyte ID No 866043CD1 30 Met Leu Leu Ser Thr Ser Met Asp Lys Thr Phe Lys Val Trp Asn 1 5 10 15 Ala Val Asp Ser Gly His Cys Leu Gln Thr Tyr Ser Leu His Thr 20 25 30 Glu Ala Val Arg Ala Ala Arg Trp Ala Pro Cys Gly Arg Arg Ile 35 40 45 Leu Ser Gly Gly Phe Asp Phe Ala Leu His Leu Thr Asp Leu Glu 50 55 60 Thr Gly Thr Gln Leu Phe Ser Gly Arg Ser Asp Phe Arg Ile Thr 65 70 75 Thr Leu Lys Phe His Pro Lys Asp His Asn Ile Phe Leu Cys Gly 80 85 90 Gly Phe Ser Ser Glu Met Lys Ala Trp Asp Ile Arg Thr Gly Lys 95 100 105 Val Met Arg Ser Tyr Lys Ala Thr Ile Gln Gln Thr Leu Asp Ile 110 115 120 Leu Phe Leu Arg Glu Gly Ser Glu Phe Leu Ser Ser Thr Asp Ala 125 130 135 Ser Thr Arg Asp Ser Ala Asp Arg Thr Ile Ile Ala Trp Asp Phe 140 145 150 Arg Thr Ser Ala Lys Ile Ser Asn Gln Ile Phe His Glu Arg Phe 155 160 165 Thr Cys Pro Ser Leu Ala Leu His Pro Arg Glu Pro Val Phe Leu 170 175 180 Ala Gln Thr Asn Gly Asn Tyr Leu Ala Leu Phe Ser Thr Val Trp 185 190 195 Pro Tyr Arg Met Ser Arg Arg Arg Arg Tyr Glu Gly His Lys Val 200 205 210 Glu Gly Tyr Ser Val Gly Cys Glu Cys Ser Pro Gly Gly Asp Leu 215 220 225 Leu Val Thr Gly Ser Ala Asp Gly Arg Val Leu Met Tyr Ser Phe 230 235 240 Arg Thr Ala Ser Arg Ala Cys Thr Leu Gln Gly His Thr Gln Ala 245 250 255 Cys Val Gly Thr Thr Tyr His Pro Val Leu Pro Ser Val Leu Ala 260 265 270 Thr Cys Ser Trp Gly Gly Asp Met Lys Ile Trp His 275 280 31 125 PRT Homo sapiens misc_feature Incyte ID No 927065CD1 31 Met Pro Ala Pro Ala Ala Thr Tyr Glu Arg Val Val Tyr Lys Asn 1 5 10 15 Pro Ser Glu Tyr His Tyr Met Lys Val Cys Leu Glu Phe Gln Asp 20 25 30 Cys Gly Val Gly Leu Asn Ala Ala Gln Phe Lys Gln Leu Leu Ile 35 40 45 Ser Ala Val Lys Asp Leu Phe Gly Glu Val Asp Ala Ala Leu Pro 50 55 60 Leu Asp Ile Leu Thr Tyr Glu Glu Lys Thr Leu Ser Ala Ile Leu 65 70 75 Arg Ile Cys Ser Ser Gly Leu Val Lys Leu Trp Ser Ser Leu Thr 80 85 90 Leu Leu Arg Ile Pro Ile Lys Gly Lys Lys Cys Ala Phe Arg Val 95 100 105 Ile Gln Val Ser Pro Phe Leu Leu Ala Leu Ser Gly Asn Ser Arg 110 115 120 Glu Leu Val Leu Asp 125 32 365 PRT Homo sapiens misc_feature Incyte ID No 938071CD1 32 Met Ala Pro Val Ser Gly Ser Arg Ser Pro Asp Arg Glu Ala Ser 1 5 10 15 Gly Ser Gly Gly Arg Arg Arg Ser Ser Ser Lys Ser Pro Lys Pro 20 25 30 Ser Lys Ser Ala Arg Ser Pro Arg Gly Arg Arg Ser Arg Ser His 35 40 45 Ser Cys Ser Arg Ser Gly Asp Arg Asn Gly Leu Thr His Gln Leu 50 55 60 Gly Gly Leu Ser Gln Gly Ser Arg Asn Gln Ser Tyr Arg Ser Arg 65 70 75 Ser Arg Ser Arg Ser Arg Glu Arg Pro Ser Ala Pro Arg Gly Ile 80 85 90 Pro Phe Ala Ser Ala Ser Ser Ser Val Tyr Tyr Gly Ser Tyr Ser 95 100 105 Arg Pro Tyr Gly Ser Asp Lys Pro Trp Pro Ser Leu Leu Asp Lys 110 115 120 Glu Arg Glu Glu Ser Leu Arg Gln Lys Arg Leu Ser Glu Arg Glu 125 130 135 Arg Ile Gly Glu Leu Gly Ala Pro Glu Val Trp Gly Leu Ser Pro 140 145 150 Lys Asn Pro Glu Pro Asp Ser Asp Glu His Thr Pro Val Glu Asp 155 160 165 Glu Glu Pro Lys Lys Ser Thr Thr Ser Ala Ser Thr Ser Glu Glu 170 175 180 Glu Lys Lys Lys Lys Ser Ser Arg Ser Lys Glu Arg Ser Lys Lys 185 190 195 Arg Arg Lys Lys Lys Ser Ser Lys Arg Lys His Lys Lys Tyr Ser 200 205 210 Glu Asp Ser Asp Ser Asp Ser Asp Ser Glu Thr Asp Ser Ser Asp 215 220 225 Glu Asp Asn Lys Arg Arg Ala Lys Lys Ala Lys Lys Lys Glu Lys 230 235 240 Lys Lys Lys His Arg Ser Lys Lys Tyr Lys Lys Lys Arg Ser Lys 245 250 255 Lys Ser Arg Lys Glu Ser Ser Asp Ser Ser Ser Lys Glu Ser Gln 260 265 270 Glu Glu Phe Leu Glu Asn Pro Trp Lys Asp Arg Thr Lys Ala Glu 275 280 285 Glu Pro Ser Asp Leu Ile Gly Pro Glu Ala Pro Lys Thr Leu Thr 290 295 300 Ser Gln Asp Asp Lys Pro Leu Lys His Arg Arg Met Glu Ala Val 305 310 315 Arg Leu Arg Lys Glu Asn Gln Ile Tyr Ser Ala Asp Glu Lys Arg 320 325 330 Ala Leu Ala Ser Phe Asn Gln Glu Glu Arg Arg Lys Arg Glu Asn 335 340 345 Lys Ile Leu Ala Ser Phe Arg Glu Met Val Tyr Arg Lys Thr Lys 350 355 360 Gly Lys Asp Asp Lys 365 33 672 PRT Homo sapiens misc_feature Incyte ID No 3295984CD1 33 Met Arg Ser Ile Arg Ser Phe Ala Asn Asp Asp Arg His Val Met 1 5 10 15 Val Lys His Ser Thr Ile Tyr Pro Ser Pro Glu Glu Leu Glu Ala 20 25 30 Val Gln Asn Met Val Ser Thr Val Glu Cys Ala Leu Lys His Val 35 40 45 Ser Asp Trp Leu Asp Glu Thr Asn Lys Gly Thr Lys Thr Glu Gly 50 55 60 Glu Thr Glu Val Lys Lys Asp Glu Ala Gly Glu Asn Tyr Ser Lys 65 70 75 Asp Gln Gly Gly Arg Thr Leu Cys Gly Val Met Arg Ile Gly Leu 80 85 90 Val Ala Lys Gly Leu Leu Ile Lys Asp Asp Met Asp Leu Glu Leu 95 100 105 Val Leu Met Cys Lys Asp Lys Pro Thr Glu Thr Leu Leu Asn Thr 110 115 120 Val Lys Asp Asn Leu Pro Ile Gln Ile Gln Lys Leu Thr Glu Glu 125 130 135 Lys Tyr Gln Val Glu Gln Cys Val Asn Glu Ala Ser Ile Ile Ile 140 145 150 Arg Asn Thr Lys Glu Pro Thr Leu Thr Leu Lys Val Ile Leu Thr 155 160 165 Ser Pro Leu Ile Arg Asp Glu Leu Glu Lys Lys Asp Gly Glu Asn 170 175 180 Val Ser Met Lys Asp Pro Pro Asp Leu Leu Asp Arg Gln Lys Cys 185 190 195 Leu Asn Ala Leu Ala Ser Leu Arg His Ala Lys Trp Phe Gln Ala 200 205 210 Arg Ala Asn Gly Leu Lys Ser Cys Val Ile Val Leu Arg Ile Leu 215 220 225 Arg Asp Leu Cys Asn Arg Val Pro Thr Trp Ala Pro Leu Lys Gly 230 235 240 Trp Pro Leu Glu Leu Ile Cys Glu Lys Ser Ile Gly Thr Cys Asn 245 250 255 Arg Pro Leu Gly Ala Gly Glu Ala Leu Arg Arg Val Met Glu Cys 260 265 270 Leu Ala Ser Gly Ile Leu Leu Pro Gly Gly Pro Gly Leu His Asp 275 280 285 Pro Cys Glu Arg Asp Pro Thr Asp Ala Leu Ser Tyr Met Thr Ile 290 295 300 Gln Gln Lys Glu Asp Ile Thr His Ser Ala Gln His Ala Leu Arg 305 310 315 Leu Ser Ala Phe Gly Gln Ile Tyr Lys Val Leu Glu Met Asp Pro 320 325 330 Leu Pro Ser Ser Lys Pro Phe Gln Lys Tyr Ser Trp Ser Val Thr 335 340 345 Asp Lys Glu Gly Ala Gly Ser Ser Ala Leu Lys Arg Pro Phe Glu 350 355 360 Asp Gly Leu Gly Asp Asp Lys Asp Pro Asn Lys Lys Met Lys Arg 365 370 375 Asn Leu Arg Lys Ile Leu Asp Ser Lys Ala Ile Asp Leu Met Asn 380 385 390 Ala Leu Met Arg Leu Asn Gln Ile Arg Pro Gly Leu Gln Tyr Lys 395 400 405 Leu Leu Ser Gln Ser Gly Pro Val His Ala Pro Val Phe Thr Met 410 415 420 Ser Val Asp Val Asp Gly Thr Thr Tyr Glu Ala Ser Gly Pro Ser 425 430 435 Lys Lys Thr Ala Lys Leu His Val Ala Val Lys Val Leu Gln Ala 440 445 450 Met Gly Tyr Pro Thr Gly Phe Asp Ala Asp Ile Glu Cys Met Ser 455 460 465 Ser Asp Glu Lys Ser Asp Asn Glu Ser Lys Asn Glu Thr Val Ser 470 475 480 Ser Asn Ser Ser Asn Asn Thr Gly Asn Ser Thr Thr Glu Thr Ser 485 490 495 Ser Thr Leu Glu Val Arg Thr Gln Gly Pro Ile Leu Thr Ala Ser 500 505 510 Gly Lys Asn Pro Val Met Glu Leu Asn Glu Lys Arg Arg Gly Leu 515 520 525 Lys Tyr Glu Leu Ile Ser Glu Thr Gly Gly Ser His Asp Lys Arg 530 535 540 Phe Val Met Glu Val Glu Val Asp Gly Gln Lys Phe Arg Gly Ala 545 550 555 Gly Pro Asn Lys Lys Val Ala Lys Ala Ser Ala Ala Leu Ala Ala 560 565 570 Leu Glu Lys Leu Phe Ser Gly Pro Asn Ala Ala Asn Asn Lys Lys 575 580 585 Lys Lys Ile Ile Pro Gln Ala Lys Gly Val Val Asn Thr Ala Val 590 595 600 Ser Ala Ala Val Gln Ala Val Arg Gly Arg Gly Arg Gly Thr Leu 605 610 615 Thr Arg Gly Ala Phe Val Gly Ala Thr Ala Ala Pro Gly Tyr Ile 620 625 630 Ala Pro Gly Tyr Gly Thr Pro Tyr Gly Tyr Ser Thr Ala Ala Pro 635 640 645 Ala Tyr Gly Leu Pro Lys Arg Met Val Leu Leu Pro Val Met Lys 650 655 660 Phe Pro Thr Tyr Pro Val Pro His Tyr Ser Phe Phe 665 670 34 430 PRT Homo sapiens misc_feature Incyte ID No 4545237CD1 34 Met Ala Thr Ala Val Arg Ala Val Gly Cys Leu Pro Val Leu Cys 1 5 10 15 Ser Gly Thr Ala Gly His Leu Leu Gly Arg Gln Cys Ser Leu Asn 20 25 30 Thr Leu Pro Ala Ala Ser Ile Leu Ala Trp Lys Ser Val Leu Gly 35 40 45 Asn Gly His Leu Ser Ser Leu Gly Thr Arg Asp Thr His Pro Tyr 50 55 60 Ala Ser Leu Ser Arg Ala Leu Gln Thr Gln Cys Cys Ile Ser Ser 65 70 75 Pro Ser His Leu Met Ser Gln Gln Tyr Arg Pro Tyr Ser Phe Phe 80 85 90 Thr Lys Leu Thr Ala Asp Glu Leu Trp Lys Gly Ala Leu Ala Glu 95 100 105 Thr Gly Ala Gly Ala Lys Lys Gly Arg Gly Lys Arg Thr Lys Lys 110 115 120 Lys Lys Arg Lys Asp Leu Asn Arg Gly Gln Ile Ile Gly Glu Gly 125 130 135 Arg Tyr Gly Phe Leu Trp Pro Gly Leu Asn Val Pro Leu Met Lys 140 145 150 Asn Gly Ala Val Gln Thr Ile Ala Gln Arg Ser Lys Glu Glu Gln 155 160 165 Glu Lys Val Glu Ala Asp Met Ile Gln Gln Arg Glu Glu Trp Asp 170 175 180 Arg Lys Lys Lys Met Lys Val Lys Arg Glu Arg Gly Trp Ser Gly 185 190 195 Asn Ser Trp Gly Gly Ile Ser Leu Gly Pro Pro Asp Pro Gly Pro 200 205 210 Cys Gly Glu Thr Tyr Glu Asp Phe Asp Thr Arg Ile Leu Glu Val 215 220 225 Arg Asn Val Phe Thr Met Thr Ala Lys Glu Gly Arg Lys Lys Ser 230 235 240 Ile Arg Val Leu Val Ala Val Gly Asn Gly Lys Gly Ala Ala Gly 245 250 255 Phe Ser Ile Gly Lys Ala Thr Asp Arg Met Asp Ala Phe Arg Lys 260 265 270 Ala Lys Asn Arg Ala Val His His Leu His Tyr Ile Glu Arg Tyr 275 280 285 Glu Asp His Thr Ile Phe His Asp Ile Ser Leu Arg Phe Lys Arg 290 295 300 Thr His Ile Lys Met Lys Lys Gln Pro Lys Gly Tyr Gly Leu Arg 305 310 315 Cys His Arg Ala Ile Ile Thr Ile Cys Arg Leu Ile Gly Ile Lys 320 325 330 Asp Met Tyr Ala Lys Val Ser Gly Ser Ile Asn Met Leu Ser Leu 335 340 345 Thr Gln Gly Leu Phe Arg Gly Leu Ser Arg Gln Glu Thr His Gln 350 355 360 Gln Leu Ala Asp Lys Lys Gly Leu His Val Val Glu Ile Arg Glu 365 370 375 Glu Cys Gly Pro Leu Pro Ile Val Val Ala Ser Pro Arg Gly Pro 380 385 390 Leu Arg Lys Asp Pro Glu Pro Glu Asp Glu Val Pro Asp Val Lys 395 400 405 Leu Asp Trp Glu Asp Val Lys Thr Ala Gln Gly Met Lys Arg Ser 410 415 420 Val Trp Ser Asn Leu Lys Arg Ala Ala Thr 425 430 35 137 PRT Homo sapiens misc_feature Incyte ID No 4942964CD1 35 Met Ala Asp Ser Lys Ala Thr Ser Ala Val Thr Leu Arg Thr Arg 1 5 10 15 Lys Phe Met Thr Asn Arg Leu Leu Ala Arg Lys Gln Phe Val Leu 20 25 30 Glu Val Ile His Pro Gly Arg Ala Asn Val Ser Lys Ala Glu Leu 35 40 45 Lys Glu Arg Leu Ala Lys Ala Tyr Glu Val Lys Asp Pro Asn Thr 50 55 60 Ile Phe Val Phe Lys Phe Arg Thr His Phe Gly Gly Gly Lys Ser 65 70 75 Thr Gly Phe Gly Leu Ile Tyr Asp Asn Leu Glu Ala Ala Lys Lys 80 85 90 Phe Glu Pro Lys Tyr Arg Leu Ile Arg Asn Gly Leu Ala Thr Lys 95 100 105 Val Glu Lys Ser Arg Lys Gln Met Lys Glu Arg Lys Asn Arg Ala 110 115 120 Lys Lys Ile Arg Gly Val Lys Lys Thr Lys Ala Gly Asp Ala Lys 125 130 135 Lys Lys 36 380 PRT Homo sapiens misc_feature Incyte ID No 5702144CD1 36 Met Arg Ser Arg Val Leu Trp Gly Ala Ala Arg Trp Leu Trp Pro 1 5 10 15 Arg Arg Ala Val Gly Pro Ala Arg Arg Pro Leu Ser Ser Gly Ser 20 25 30 Pro Pro Leu Glu Glu Leu Phe Thr Arg Gly Gly Pro Leu Arg Thr 35 40 45 Phe Leu Glu Arg Gln Ala Gly Ser Glu Ala His Leu Lys Val Arg 50 55 60 Arg Pro Glu Leu Leu Ala Val Ile Lys Leu Leu Asn Glu Lys Glu 65 70 75 Gln Glu Leu Arg Glu Thr Glu His Leu Leu His Asp Glu Asn Glu 80 85 90 Asp Leu Arg Lys Leu Ala Glu Asn Glu Ile Thr Leu Cys Gln Lys 95 100 105 Glu Ile Thr Gln Leu Lys His Gln Ile Ile Leu Leu Leu Val Pro 110 115 120 Ser Glu Glu Thr Asp Glu Asn Asp Leu Ile Leu Glu Val Thr Ala 125 130 135 Gly Val Gly Gly Gln Glu Ala Met Leu Phe Thr Ser Glu Ile Phe 140 145 150 Asp Met Tyr Gln Gln Tyr Ala Ala Phe Lys Arg Trp His Phe Glu 155 160 165 Thr Leu Glu Tyr Phe Pro Ser Glu Leu Gly Gly Leu Arg His Ala 170 175 180 Ser Ala Ser Ile Gly Gly Ser Glu Ala Tyr Arg His Met Lys Phe 185 190 195 Glu Gly Gly Val His Arg Val Gln Arg Val Pro Lys Thr Glu Lys 200 205 210 Gln Gly Arg Ile His Thr Ser Thr Met Thr Val Ala Ile Leu Pro 215 220 225 Gln Pro Thr Glu Ile Asn Leu Val Ile Asn Pro Lys Asp Leu Arg 230 235 240 Ile Asp Thr Lys Arg Ala Ser Gly Ala Gly Gly Gln His Val Asn 245 250 255 Thr Thr Asp Ser Ala Val Arg Ile Val His Leu Pro Thr Gly Val 260 265 270 Val Ser Glu Cys Gln Gln Glu Arg Ser Gln Leu Lys Asn Lys Glu 275 280 285 Leu Ala Met Thr Lys Leu Arg Ala Lys Leu Tyr Ser Met His Leu 290 295 300 Glu Glu Glu Ile Asn Lys Arg Gln Asn Ala Arg Lys Ile Gln Ile 305 310 315 Gly Ser Lys Gly Arg Ser Glu Lys Ile Arg Thr Tyr Asn Phe Pro 320 325 330 Gln Asn Arg Val Thr Asp His Arg Ile Asn Lys Thr Leu His Asp 335 340 345 Leu Glu Thr Phe Met Gln Gly Asp Tyr Leu Leu Asp Glu Leu Val 350 355 360 Gln Ser Leu Lys Glu Tyr Ala Asp Tyr Glu Ser Leu Val Glu Ile 365 370 375 Ile Ser Gln Lys Val 380 37 206 PRT Homo sapiens misc_feature Incyte ID No 5862945CD1 37 Met Ala Ala Ala Val Leu Gly Gln Leu Gly Ala Leu Trp Ile His 1 5 10 15 Asn Leu Arg Ser Arg Gly Lys Leu Ala Leu Gly Val Leu Pro Gln 20 25 30 Ser Tyr Ile His Thr Ser Ala Ser Leu Asp Ile Ser Arg Lys Trp 35 40 45 Glu Lys Lys Asn Lys Ile Val Tyr Pro Pro Gln Leu Pro Gly Glu 50 55 60 Pro Arg Arg Pro Ala Glu Ile Tyr His Cys Arg Arg Gln Ile Lys 65 70 75 Tyr Ser Lys Asp Lys Met Trp Tyr Leu Ala Lys Leu Ile Arg Gly 80 85 90 Met Ser Ile Asp Gln Ala Leu Ala Gln Leu Glu Phe Asn Asp Lys 95 100 105 Lys Gly Ala Lys Ile Ile Lys Glu Val Leu Leu Glu Ala Gln Asp 110 115 120 Met Ala Val Arg Asp His Asn Val Glu Phe Arg Ser Asn Leu Tyr 125 130 135 Ile Ala Glu Ser Thr Ser Gly Arg Gly Gln Cys Leu Lys Arg Ile 140 145 150 Arg Tyr His Gly Arg Gly Arg Phe Gly Ile Met Glu Lys Val Tyr 155 160 165 Cys His Tyr Phe Val Lys Leu Val Glu Gly Pro Pro Pro Pro Pro 170 175 180 Glu Pro Pro Lys Thr Ala Val Ala His Ala Lys Glu Tyr Ile Gln 185 190 195 Gln Leu Arg Ser Arg Thr Ile Val His Thr Leu 200 205 38 190 PRT Homo sapiens misc_feature Incyte ID No 6319547CD1 38 Met Glu Ala Glu Thr Lys Thr Leu Pro Leu Glu Asn Ala Ser Ile 1 5 10 15 Leu Ser Glu Gly Ser Leu Gln Glu Gly His Arg Leu Trp Ile Gly 20 25 30 Asn Leu Asp Pro Lys Ile Thr Glu Tyr His Leu Leu Lys Leu Leu 35 40 45 Gln Lys Phe Gly Lys Val Lys Gln Phe Asp Phe Leu Phe His Lys 50 55 60 Ser Gly Ala Leu Glu Gly Gln Pro Arg Gly Tyr Cys Phe Val Asn 65 70 75 Phe Glu Thr Lys Gln Glu Ala Glu Gln Ala Ile Gln Cys Leu Asn 80 85 90 Gly Lys Leu Ala Leu Ser Lys Lys Leu Val Val Arg Trp Ala His 95 100 105 Ala Gln Val Lys Arg Tyr Asp His Asn Lys Asn Asp Lys Ile Leu 110 115 120 Pro Ile Ser Leu Glu Pro Ser Ser Ser Thr Glu Pro Thr Gln Ser 125 130 135 Asn Leu Ser Val Thr Ala Lys Ile Lys Ala Ile Glu Ala Lys Leu 140 145 150 Lys Met Met Ala Glu Asn Pro Asp Ala Glu Tyr Pro Ala Ala Pro 155 160 165 Val Tyr Ser Tyr Phe Lys Pro Pro Asp Lys Lys Arg Thr Thr Pro 170 175 180 Tyr Ser Arg Thr Ala Trp Lys Ser Arg Arg 185 190 39 434 PRT Homo sapiens misc_feature Incyte ID No 000124CD1 39 Met Leu Arg Cys Leu Tyr His Trp His Arg Pro Val Leu Asn Arg 1 5 10 15 Arg Trp Ser Arg Leu Cys Leu Leu Lys Gln Tyr Leu Phe Thr Met 20 25 30 Lys Leu Gln Ser Pro Glu Phe Gln Ser Leu Phe Thr Glu Gly Leu 35 40 45 Lys Ser Leu Thr Glu Leu Phe Val Lys Glu Asn His Glu Leu Arg 50 55 60 Ile Ala Gly Gly Ala Val Arg Asp Leu Leu Asn Gly Val Lys Pro 65 70 75 Gln Asp Ile Asp Phe Ala Thr Thr Ala Thr Pro Thr Gln Met Lys 80 85 90 Glu Met Phe Gln Ser Ala Gly Ile Arg Met Ile Asn Asn Arg Gly 95 100 105 Glu Lys His Gly Thr Ile Thr Ala Arg Leu His Glu Glu Asn Phe 110 115 120 Glu Ile Thr Thr Leu Arg Ile Asp Val Thr Thr Asp Gly Arg His 125 130 135 Ala Glu Val Glu Phe Thr Thr Asp Trp Gln Lys Asp Ala Glu Arg 140 145 150 Arg Asp Leu Thr Ile Asn Ser Met Phe Leu Gly Phe Asp Gly Thr 155 160 165 Leu Phe Asp Tyr Phe Asn Gly Tyr Glu Asp Leu Lys Asn Lys Lys 170 175 180 Val Arg Phe Val Gly His Ala Lys Gln Arg Ile Gln Glu Asp Tyr 185 190 195 Leu Arg Ile Leu Arg Tyr Phe Arg Phe Tyr Gly Arg Ile Val Asp 200 205 210 Lys Pro Gly Asp His Asp Pro Glu Thr Leu Glu Ala Ile Ala Glu 215 220 225 Asn Ala Lys Gly Leu Ala Gly Ile Ser Gly Glu Arg Ile Trp Val 230 235 240 Glu Leu Lys Lys Ile Leu Val Gly Asn His Val Asn His Leu Ile 245 250 255 His Leu Ile Tyr Asp Leu Asp Val Ala Pro Tyr Ile Gly Leu Pro 260 265 270 Ala Asn Ala Ser Leu Glu Glu Phe Asp Lys Val Ser Lys Asn Val 275 280 285 Asp Gly Phe Ser Pro Lys Pro Val Thr Leu Leu Ala Ser Leu Phe 290 295 300 Lys Val Gln Asp Asp Val Thr Lys Leu Asp Leu Arg Leu Lys Ile 305 310 315 Ala Lys Glu Glu Lys Asn Leu Gly Leu Phe Ile Val Lys Asn Arg 320 325 330 Lys Asp Leu Ile Lys Ala Thr Asp Ser Ser Asp Pro Leu Lys Pro 335 340 345 Tyr Gln Asp Phe Ile Ile Asp Ser Arg Glu Pro Asp Ala Thr Thr 350 355 360 Arg Val Cys Glu Leu Leu Lys Tyr Gln Gly Glu His Cys Leu Leu 365 370 375 Lys Glu Met Gln Gln Trp Ser Ile Pro Pro Phe Pro Val Ser Gly 380 385 390 His Asp Ile Arg Lys Val Gly Ile Ser Ser Gly Lys Glu Ile Gly 395 400 405 Ala Leu Leu Gln Gln Leu Arg Glu Gln Trp Lys Lys Ser Gly Tyr 410 415 420 Gln Met Glu Lys Asp Glu Leu Leu Ser Tyr Ile Lys Lys Thr 425 430 40 339 PRT Homo sapiens misc_feature Incyte ID No 1659474CD1 40 Met Ala Ala Gly Cys Ser Glu Ala Pro Arg Pro Thr Ala Ala Ser 1 5 10 15 Asp Gly Ser Leu Val Gly Gln Ala Gly Val Leu Pro Cys Leu Glu 20 25 30 Leu Pro Thr Tyr Ala Ala Ala Cys Ala Leu Val Asn Ser Arg Tyr 35 40 45 Ser Cys Leu Val Ala Gly Pro His Gln Arg His Ile Ala Leu Ser 50 55 60 Pro Arg Tyr Leu Asn Arg Lys Arg Thr Gly Ile Arg Glu Gln Leu 65 70 75 Asp Ala Glu Leu Leu Arg Tyr Ser Glu Ser Leu Leu Gly Val Pro 80 85 90 Ile Ala Tyr Asp Asn Ile Lys Val Val Gly Glu Leu Gly Asp Ile 95 100 105 Tyr Asp Asp Gln Gly His Ile His Leu Asn Ile Glu Ala Asp Phe 110 115 120 Val Ile Phe Cys Pro Glu Pro Gly Gln Lys Leu Met Gly Ile Val 125 130 135 Asn Lys Val Ser Ser Ser His Ile Gly Cys Leu Val His Gly Cys 140 145 150 Phe Asn Ala Ser Ile Pro Lys Pro Glu Gln Leu Ser Ala Glu Gln 155 160 165 Trp Gln Thr Met Glu Ile Asn Met Gly Asp Glu Leu Glu Phe Glu 170 175 180 Val Phe Arg Leu Asp Ser Asp Ala Ala Gly Val Phe Cys Ile Arg 185 190 195 Gly Lys Leu Asn Ile Thr Ser Leu Gln Phe Lys Arg Ser Glu Val 200 205 210 Ser Glu Glu Val Thr Glu Asn Gly Thr Glu Glu Ala Ala Lys Lys 215 220 225 Pro Lys Lys Lys Lys Lys Lys Lys Asp Pro Glu Thr Tyr Glu Val 230 235 240 Asp Ser Gly Thr Thr Lys Leu Ala Asp Asp Ala Asp Asp Thr Pro 245 250 255 Met Glu Glu Ser Ala Leu Gln Asn Thr Asn Asn Ala Asn Gly Ile 260 265 270 Trp Glu Glu Glu Pro Lys Lys Lys Lys Lys Lys Lys Lys His Gln 275 280 285 Glu Val Gln Asp Gln Asp Pro Val Phe Gln Gly Ser Asp Ser Ser 290 295 300 Gly Tyr Gln Ser Asp His Lys Lys Lys Lys Lys Glu Lys Lys Thr 305 310 315 Asn Ser Glu Glu Ala Glu Phe Thr Pro Pro Leu Lys Cys Ser Pro 320 325 330 Lys Arg Lys Gly Lys Ser Asn Phe Leu 335 41 599 PRT Homo sapiens misc_feature Incyte ID No 2267892CD1 41 Met Asp Val His Asp Leu Phe Arg Arg Leu Gly Ala Gly Ala Lys 1 5 10 15 Phe Asp Thr Arg Arg Phe Ser Ala Asp Ala Ala Arg Phe Gln Ile 20 25 30 Gly Lys Arg Lys Tyr Asp Phe Asp Ser Ser Glu Val Leu Gln Gly 35 40 45 Leu Asp Phe Phe Gly Asn Lys Lys Ser Val Pro Gly Val Cys Gly 50 55 60 Ala Ser Gln Thr His Gln Lys Pro Gln Asn Gly Glu Lys Lys Glu 65 70 75 Glu Ser Leu Thr Glu Arg Lys Arg Glu Gln Ser Lys Lys Lys Arg 80 85 90 Lys Thr Met Thr Ser Glu Ile Ala Ser Gln Glu Glu Gly Ala Thr 95 100 105 Ile Gln Trp Met Ser Ser Val Glu Ala Lys Ile Glu Asp Lys Lys 110 115 120 Val Gln Arg Glu Ser Lys Leu Thr Ser Gly Lys Leu Glu Asn Leu 125 130 135 Arg Lys Glu Lys Ile Asn Phe Leu Arg Asn Lys His Lys Ile His 140 145 150 Val Gln Gly Thr Asp Leu Pro Asp Pro Ile Ala Thr Phe Gln Gln 155 160 165 Leu Asp Gln Glu Tyr Lys Ile Asn Ser Arg Leu Leu Gln Asn Ile 170 175 180 Leu Asp Ala Gly Phe Gln Met Pro Thr Pro Ile Gln Met Gln Ala 185 190 195 Ile Pro Val Met Leu His Gly Arg Glu Leu Leu Ala Ser Ala Pro 200 205 210 Thr Gly Ser Gly Lys Thr Leu Ala Phe Ser Ile Pro Ile Leu Met 215 220 225 Gln Leu Lys Gln Pro Ala Asn Lys Gly Phe Arg Ala Leu Ile Ile 230 235 240 Ser Pro Thr Arg Glu Leu Ala Ser Gln Ile His Arg Glu Leu Ile 245 250 255 Lys Ile Ser Glu Gly Thr Gly Phe Arg Ile His Met Ile His Lys 260 265 270 Ala Ala Val Ala Ala Lys Lys Phe Gly Pro Lys Ser Ser Lys Lys 275 280 285 Phe Asp Ile Leu Val Thr Thr Pro Asn Arg Leu Ile Tyr Leu Leu 290 295 300 Lys Gln Asp Pro Pro Gly Ile Asp Leu Ala Ser Val Glu Trp Leu 305 310 315 Val Val Asp Glu Ser Asp Lys Leu Phe Glu Asp Gly Lys Thr Gly 320 325 330 Phe Arg Asp Gln Leu Ala Ser Ile Phe Leu Ala Cys Thr Ser His 335 340 345 Lys Val Arg Arg Ala Met Phe Ser Ala Thr Phe Ala Tyr Asp Val 350 355 360 Glu Gln Trp Cys Lys Leu Asn Leu Asp Asn Val Ile Ser Val Ser 365 370 375 Ile Gly Ala Arg Asn Ser Ala Val Glu Thr Val Glu Gln Glu Leu 380 385 390 Leu Phe Val Gly Ser Glu Thr Gly Lys Leu Leu Ala Met Arg Glu 395 400 405 Leu Val Lys Lys Gly Phe Asn Pro Pro Val Leu Val Phe Val Gln 410 415 420 Ser Ile Glu Arg Ala Lys Glu Leu Phe His Glu Leu Ile Tyr Glu 425 430 435 Gly Ile Asn Val Asp Val Ile His Ala Glu Arg Thr Gln Gln Gln 440 445 450 Arg Asp Asn Thr Val His Ser Phe Arg Ala Gly Lys Ile Trp Val 455 460 465 Leu Ile Cys Thr Ala Leu Leu Ala Arg Gly Ile Asp Phe Lys Gly 470 475 480 Val Asn Leu Val Ile Asn Tyr Asp Phe Pro Thr Ser Ser Val Glu 485 490 495 Tyr Ile His Arg Ile Gly Arg Thr Gly Arg Ala Gly Asn Lys Gly 500 505 510 Lys Ala Ile Thr Phe Phe Thr Glu Asp Asp Lys Pro Leu Leu Arg 515 520 525 Ser Val Ala Asn Val Ile Gln Gln Ala Gly Cys Pro Val Pro Glu 530 535 540 Tyr Ile Lys Gly Phe Gln Lys Leu Leu Ser Lys Gln Lys Lys Lys 545 550 555 Met Ile Lys Lys Pro Leu Glu Arg Glu Ser Ile Ser Thr Thr Pro 560 565 570 Lys Cys Phe Leu Glu Lys Ala Lys Asp Lys Gln Lys Lys Val Thr 575 580 585 Gly Gln Asn Ser Lys Lys Lys Val Ala Leu Glu Asp Lys Ser 590 595 42 334 PRT Homo sapiens misc_feature Incyte ID No 2670307CD1 42 Met Ala Ala Ser Gly Ser Gly Met Ala Gln Lys Thr Trp Glu Leu 1 5 10 15 Ala Asn Asn Met Gln Glu Ala Gln Ser Ile Asp Glu Ile Tyr Lys 20 25 30 Tyr Asp Lys Lys Gln Gln Gln Glu Ile Leu Ala Ala Lys Pro Gly 35 40 45 Leu Arg Ile His His Tyr Phe Lys Tyr Cys Lys Ile Ser Ala Leu 50 55 60 Ala Leu Leu Lys Met Val Met His Ala Arg Ser Gly Gly Asn Leu 65 70 75 Glu Val Met Gly Leu Met Leu Gly Lys Val Asp Gly Glu Thr Met 80 85 90 Ile Ile Met Asp Ser Phe Ala Leu Pro Val Glu Gly Thr Glu Thr 95 100 105 Arg Val Asn Ala Gln Ala Ala Ala Tyr Glu Tyr Met Ala Ala Tyr 110 115 120 Ile Glu Asn Ala Lys Gln Val Gly Arg Leu Glu Asn Ala Ile Gly 125 130 135 Trp Tyr His Ser His Pro Gly Tyr Gly Cys Trp Leu Ser Gly Ile 140 145 150 Asp Val Ser Thr Gln Met Leu Asn Gln Gln Phe Gln Glu Pro Phe 155 160 165 Val Ala Val Val Ile Asp Pro Thr Arg Thr Ile Ser Ala Gly Lys 170 175 180 Val Asn Leu Gly Ala Phe Arg Thr Tyr Pro Lys Gly Tyr Lys Pro 185 190 195 Pro Asp Glu Gly Pro Ser Glu Tyr Gln Thr Ile Pro Leu Asn Lys 200 205 210 Ile Glu Asp Phe Gly Val His Cys Lys Gln Tyr Tyr Ala Leu Glu 215 220 225 Val Ser Tyr Phe Lys Ser Ser Leu Asp Arg Lys Leu Leu Glu Leu 230 235 240 Leu Trp Asn Lys Tyr Trp Val Asn Thr Leu Ser Ser Ser Ser Leu 245 250 255 Leu Thr Asn Ala Asp Tyr Thr Thr Gly Gln Val Phe Asp Leu Ser 260 265 270 Glu Lys Leu Glu Gln Ser Glu Ala Gln Leu Gly Arg Gly Ser Phe 275 280 285 Met Leu Gly Leu Glu Thr His Asp Arg Lys Ser Glu Asp Lys Leu 290 295 300 Ala Lys Ala Thr Arg Asp Ser Cys Lys Thr Thr Ile Glu Ala Ile 305 310 315 His Gly Leu Met Ser Gln Val Ile Lys Asp Lys Leu Phe Asn Gln 320 325 330 Ile Asn Ile Ser 43 448 PRT Homo sapiens misc_feature Incyte ID No 4524210CD1 43 Met Asn Lys Glu Ile Val Thr Ala Leu Gly Lys Gln Glu Ala Glu 1 5 10 15 Arg Lys Phe Glu Thr Leu Leu Lys His Leu Ser His Pro Pro Ser 20 25 30 Phe Thr Thr Val Arg Val Asn Thr His Leu Ala Ser Val Gln His 35 40 45 Val Lys Asn Leu Leu Leu Asp Glu Leu Gln Lys Gln Phe Asn Gly 50 55 60 Leu Ser Val Pro Ile Leu Gln His Pro Asp Leu Gln Asp Val Leu 65 70 75 Leu Ile Pro Val Ile Gly Pro Arg Lys Asn Ile Lys Lys Gln Gln 80 85 90 Cys Glu Ala Ile Val Gly Ala Gln Cys Gly Asn Ala Val Leu Arg 95 100 105 Gly Ala His Val Tyr Ala Pro Gly Ile Val Ser Ala Ser Gln Phe 110 115 120 Met Lys Ala Gly Asp Val Ile Ser Val Tyr Ser Asp Ile Lys Gly 125 130 135 Lys Cys Lys Lys Gly Ala Lys Glu Phe Asp Gly Thr Lys Val Phe 140 145 150 Leu Gly Asn Gly Ile Ser Glu Leu Ser Arg Lys Glu Ile Phe Ser 155 160 165 Gly Leu Pro Glu Leu Lys Gly Met Gly Ile Arg Met Thr Glu Pro 170 175 180 Val Tyr Leu Ser Pro Ser Phe Asp Ser Val Leu Pro Arg Tyr Leu 185 190 195 Phe Leu Gln Asn Leu Pro Ser Ala Leu Val Ser His Val Leu Asn 200 205 210 Pro Gln Pro Gly Glu Lys Ile Leu Asp Leu Cys Ala Ala Pro Gly 215 220 225 Gly Lys Thr Thr His Ile Ala Ala Leu Met His Asp Gln Gly Glu 230 235 240 Val Ile Ala Leu Asp Lys Ile Phe Asn Lys Val Glu Lys Ile Lys 245 250 255 Gln Asn Ala Leu Leu Leu Gly Leu Asn Ser Ile Arg Ala Phe Cys 260 265 270 Phe Asp Gly Thr Lys Ala Val Lys Leu Asp Met Val Glu Asp Thr 275 280 285 Glu Gly Glu Pro Pro Phe Leu Pro Glu Ser Phe Asp Arg Ile Leu 290 295 300 Leu Asp Ala Pro Cys Ser Gly Met Gly Gln Arg Pro Asn Met Ala 305 310 315 Cys Thr Trp Ser Val Lys Glu Val Ala Ser Tyr Gln Pro Leu Gln 320 325 330 Arg Lys Leu Phe Thr Ala Ala Val Gln Leu Leu Lys Pro Glu Gly 335 340 345 Val Leu Val Tyr Ser Thr Cys Thr Ile Thr Leu Ala Glu Asn Glu 350 355 360 Glu Gln Val Ala Trp Ala Leu Thr Lys Phe Pro Cys Leu Gln Leu 365 370 375 Gln Pro Gln Glu Pro Gln Ile Gly Gly Glu Gly Met Arg Gly Ala 380 385 390 Gly Leu Ser Cys Glu Gln Leu Lys Gln Leu Gln Arg Phe Asp Pro 395 400 405 Ser Ala Val Pro Leu Pro Asp Thr Asp Met Asp Ser Leu Arg Glu 410 415 420 Ala Arg Arg Glu Asp Met Leu Arg Leu Ala Asn Lys Asp Ser Ile 425 430 435 Gly Phe Phe Ile Ala Lys Phe Val Lys Cys Lys Ser Thr 440 445 44 420 PRT Homo sapiens misc_feature Incyte ID No 5584860CD1 44 Met Ala Thr Ser Leu Gly Ser Asn Thr Tyr Asn Arg Gln Asn Trp 1 5 10 15 Glu Asp Ala Asp Phe Pro Ile Leu Cys Gln Thr Cys Leu Gly Glu 20 25 30 Asn Pro Tyr Ile Arg Met Thr Lys Glu Lys Tyr Gly Lys Glu Cys 35 40 45 Lys Ile Cys Ala Arg Pro Phe Thr Val Phe Arg Trp Cys Pro Gly 50 55 60 Val Arg Met Arg Phe Lys Lys Thr Glu Val Cys Gln Thr Cys Ser 65 70 75 Lys Leu Lys Asn Val Cys Gln Thr Cys Leu Leu Asp Leu Glu Tyr 80 85 90 Gly Leu Pro Ile Gln Val Arg Asp Ala Gly Leu Ser Phe Lys Asp 95 100 105 Asp Met Pro Lys Ser Asp Val Asn Lys Glu Tyr Tyr Thr Gln Asn 110 115 120 Met Glu Arg Glu Ile Ser Asn Ser Asp Gly Thr Arg Pro Val Gly 125 130 135 Met Leu Gly Lys Ala Thr Ser Thr Ser Asp Met Leu Leu Lys Leu 140 145 150 Ala Arg Thr Thr Pro Tyr Tyr Lys Arg Asn Arg Pro His Ile Cys 155 160 165 Ser Phe Trp Val Lys Gly Glu Cys Lys Arg Gly Glu Glu Cys Pro 170 175 180 Tyr Arg His Glu Lys Pro Thr Asp Pro Asp Asp Pro Leu Ala Asp 185 190 195 Gln Asn Ile Lys Asp Arg Tyr Tyr Gly Ile Asn Asp Pro Val Ala 200 205 210 Asp Lys Leu Leu Lys Arg Ala Ser Thr Met Pro Arg Leu Asp Pro 215 220 225 Pro Glu Asp Lys Thr Ile Thr Thr Leu Tyr Val Gly Gly Leu Gly 230 235 240 Asp Thr Ile Thr Glu Thr Asp Leu Arg Asn His Phe Tyr Gln Phe 245 250 255 Gly Glu Ile Arg Thr Ile Thr Val Val Gln Arg Gln Gln Cys Ala 260 265 270 Phe Ile Gln Phe Ala Thr Arg Gln Ala Ala Glu Val Ala Ala Glu 275 280 285 Lys Ser Phe Asn Lys Leu Ile Val Asn Gly Arg Arg Leu Asn Val 290 295 300 Lys Trp Gly Arg Ser Gln Ala Ala Arg Gly Lys Glu Lys Glu Lys 305 310 315 Asp Gly Thr Thr Asp Ser Gly Ile Lys Leu Glu Pro Val Pro Gly 320 325 330 Leu Pro Gly Ala Leu Pro Pro Pro Pro Ala Ala Glu Glu Glu Ala 335 340 345 Ser Ala Asn Tyr Phe Asn Leu Pro Pro Ser Gly Pro Pro Ala Val 350 355 360 Val Asn Ile Ala Leu Pro Pro Pro Pro Gly Ile Ala Pro Pro Pro 365 370 375 Pro Pro Gly Phe Gly Pro His Met Phe His Pro Met Gly Pro Pro 380 385 390 Pro Pro Phe Met Arg Ala Pro Gly Pro Ile His Tyr Pro Ser Gln 395 400 405 Asp Pro Gln Arg Met Gly Ala His Ala Gly Lys His Ser Ser Pro 410 415 420 45 137 PRT Homo sapiens misc_feature Incyte ID No 5807892CD1 45 Met Val His Leu Thr Thr Leu Leu Cys Lys Ala Tyr Arg Gly Gly 1 5 10 15 His Leu Thr Ile Arg Leu Ala Leu Gly Gly Cys Thr Asn Arg Pro 20 25 30 Phe Tyr Arg Ile Val Ala Ala His Asn Lys Cys Pro Arg Asp Gly 35 40 45 Arg Phe Val Glu Gln Leu Gly Ser Tyr Asp Pro Leu Pro Asn Ser 50 55 60 His Gly Glu Lys Leu Val Ala Leu Asn Leu Asp Arg Ile Arg His 65 70 75 Trp Ile Gly Cys Gly Ala His Leu Ser Lys Pro Met Glu Lys Leu 80 85 90 Leu Gly Leu Ala Gly Phe Phe Pro Leu His Pro Met Met Ile Thr 95 100 105 Asn Ala Glu Arg Leu Arg Arg Lys Arg Ala Arg Glu Val Leu Leu 110 115 120 Ala Ser Gln Lys Thr Asp Ala Glu Ala Thr Asp Thr Glu Ala Thr 125 130 135 Glu Thr 46 556 PRT Homo sapiens misc_feature Incyte ID No 3210044CD1 46 Met Met Asn Leu Pro Phe Asn Arg Asp Ala Val Phe Tyr His Glu 1 5 10 15 Asp Glu Thr Asn Cys Leu Leu Leu Ile Met Ala Pro Ser Phe Thr 20 25 30 Ala Arg Ile Gln Leu Phe Leu Leu Arg Ala Leu Gly Phe Leu Ile 35 40 45 Gly Leu Val Gly Arg Ala Ala Leu Val Leu Gly Gly Pro Lys Phe 50 55 60 Ala Ser Lys Thr Pro Arg Pro Val Thr Glu Pro Leu Leu Leu Leu 65 70 75 Ser Gly Met Gln Leu Ala Lys Leu Ile Arg Gln Arg Lys Val Lys 80 85 90 Cys Ile Asp Val Val Gln Ala Tyr Ile Asn Arg Ile Lys Asp Val 95 100 105 Asn Pro Met Ile Asn Gly Ile Val Lys Tyr Arg Phe Glu Glu Ala 110 115 120 Met Lys Glu Ala His Ala Val Asp Gln Lys Leu Ala Glu Lys Gln 125 130 135 Glu Asp Glu Ala Thr Leu Glu Asn Lys Trp Pro Phe Leu Gly Val 140 145 150 Pro Leu Thr Val Lys Glu Ala Phe Gln Leu Gln Gly Met Pro Asn 155 160 165 Ser Ser Gly Leu Met Asn Arg Arg Asp Ala Ile Ala Lys Thr Asp 170 175 180 Ala Thr Val Val Ala Leu Leu Lys Gly Ala Gly Ala Ile Pro Leu 185 190 195 Gly Ile Thr Asn Cys Ser Glu Leu Cys Met Trp Tyr Glu Ser Ser 200 205 210 Asn Lys Ile Tyr Gly Arg Ser Asn Asn Pro Tyr Asp Leu Gln His 215 220 225 Ile Val Gly Gly Ser Ser Gly Gly Glu Gly Cys Thr Leu Ala Ala 230 235 240 Ala Cys Ser Val Ile Gly Val Gly Ser Asp Ile Gly Gly Ser Ile 245 250 255 Arg Met Pro Ala Phe Phe Asn Gly Ile Phe Gly His Lys Pro Ser 260 265 270 Pro Gly Val Val Pro Asn Lys Gly Gln Phe Pro Leu Ala Val Gly 275 280 285 Ala Gln Glu Leu Phe Leu Cys Thr Gly Pro Met Cys Arg Tyr Ala 290 295 300 Glu Asp Leu Ala Pro Met Leu Lys Val Met Ala Gly Pro Gly Ile 305 310 315 Lys Arg Leu Lys Leu Asp Thr Lys Val His Leu Lys Asp Leu Lys 320 325 330 Phe Tyr Trp Met Glu His Asp Gly Gly Ser Phe Leu Met Ser Lys 335 340 345 Val Asp Gln Asp Leu Ile Met Thr Gln Lys Lys Val Val Val His 350 355 360 Leu Glu Thr Ile Leu Gly Ala Ser Val Gln His Val Lys Leu Lys 365 370 375 Lys Met Lys Tyr Ser Phe Gln Leu Trp Ile Ala Met Met Ser Ala 380 385 390 Lys Gly His Asp Gly Lys Glu Pro Val Lys Phe Val Asp Leu Leu 395 400 405 Gly Asp His Gly Lys His Val Ser Pro Leu Trp Glu Leu Ile Lys 410 415 420 Trp Cys Leu Gly Leu Ser Val Tyr Thr Ile Pro Ser Ile Gly Leu 425 430 435 Ala Leu Leu Glu Glu Lys Leu Arg Tyr Ser Asn Glu Lys Tyr Gln 440 445 450 Lys Phe Lys Ala Val Glu Glu Ser Leu Arg Lys Glu Leu Val Asp 455 460 465 Met Leu Gly Asp Asp Gly Val Phe Leu Tyr Pro Ser His Pro Thr 470 475 480 Val Ala Pro Lys His His Val Pro Leu Thr Arg Pro Phe Asn Phe 485 490 495 Ala Tyr Thr Gly Val Phe Ser Ala Leu Gly Leu Pro Val Thr Gln 500 505 510 Cys Pro Leu Gly Leu Asn Ala Lys Gly Leu Pro Leu Gly Ile Gln 515 520 525 Val Val Ala Gly Pro Phe Asn Asp His Leu Thr Leu Ala Val Ala 530 535 540 Gln Tyr Leu Glu Lys Thr Phe Gly Gly Trp Val Cys Pro Gly Lys 545 550 555 Phe 47 111 PRT Homo sapiens misc_feature Incyte ID No 4942454CD1 47 Met Lys Phe Val Ala Ala Tyr Leu Leu Ala Val Leu Ala Gly Asn 1 5 10 15 Ser Ser Pro Ser Ala Glu Asp Leu Thr Ala Ile Leu Glu Ser Val 20 25 30 Gly Cys Glu Val Asp Asn Glu Lys Met Glu Leu Leu Leu Ser Gln 35 40 45 Leu Ser Gly Lys Asp Ile Thr Glu Leu Ile Ala Ala Gly Arg Glu 50 55 60 Lys Phe Ala Ser Val Pro Cys Gly Gly Gly Gly Val Ala Val Ala 65 70 75 Ala Ala Ala Pro Ala Ala Gly Gly Ala Pro Ala Ala Glu Ala Lys 80 85 90 Lys Glu Glu Lys Val Glu Glu Lys Glu Glu Ser Asp Asp Asp Met 95 100 105 Gly Phe Ser Leu Phe Asp 110 48 882 DNA Homo sapiens misc_feature Incyte ID No 1622129CB1 48 cccacgcgtc cgcggagccg ccgggagctg tagttctccc gcggctcaga gaagtaggca 60 gagagcggac ctggcggccg ggcagcatgg cggggctgga gctcttgtcg gaccagggct 120 accgggtgga cgggcggcgc gccggggagc tgcgcaagat ccaggcgcgg atgggcgtgt 180 tcgcgcaggc tgacggctcg gcctacattg agcagggcaa caccaaggca ctggctgtgg 240 tctacggccc gcacgagatc cggggctccc gggctcgagc cctgccggac agggccctag 300 tgaactgtca atatagttca gcgaccttca gcacaggtga gcgcaagcga cggccacatg 360 gggaccgtaa gtcctgtgag atgggcctgc agctccgcca gactttcgaa gcagccatcc 420 tcacacagct gcacccacgc tcccagattg atatctatgt gcaggtgcta caggcagatg 480 gtgggaccta tgcagcttgt gtgaatgcag ccacgctggc agtgctggat gccgggatac 540 ccatgagaga ctttgtgtgt gcgtgctcag ctggcttcgt ggacggcaca gccctggcgg 600 acctcagcca tgtggaggaa gcagctggtg gcccccagct ggccctggcc ctgctgccag 660 cctcaggaca gattgcgctg cttgagatgg atgcccggct gcacgaggac cacctggagc 720 gggtgttgga ggctgctgcc caggctgccc gagatgtgca caccctctta gatcgagtgg 780 tccggcagca tgtgcgtgag gcctctatct tgctggggga ctgaccaccc agccacccat 840 gtccagaata aaaccctcct ctgcccacaa aaaaaaaaaa aa 882 49 1220 DNA Homo sapiens misc_feature Incyte ID No 1820078CB1 49 ctcaacttta gcccgccgga agcggaagtc aggtggttgt cggattttag aggaaggcgc 60 tcggttacat tggagaactg gagtggtctg gagttccacg gtgtagtgga ccagaggcca 120 cctctcctgg gcttctcagt gtctcgccgg cggggttcgg cctgagctgg attgacatag 180 cccttggcgg atttaaacaa cctaaacatt aagcagtaca gctgcctcaa acctttggga 240 ttttcagaat gactgacact gccgaagctg ttccaaagtt tgaagagatg tttgctagta 300 gattcacaga aaatgacaag gagtatcagg aatacctgaa acgccctcct gagtctcctc 360 caattgttga ggaatggaat agcagagctg gtgggaacca aagaaacaga ggcaatcggt 420 tgcaagacaa cagacagttc agaggcaggg acaacagatg ggggtggcca agtgacaatc 480 gatccaatca gtggcatgga cgatcctggg gtaacaacta cccgcaacac agacaagaac 540 cttactatcc ccagcaatat ggacattatg gttacaacca gcggcctcct tacggttact 600 actgatagaa atgttggcag cttttagtaa aagcatttac tctgttacca tgagaaaagt 660 ttgggtgtct tctgttggtc atagttttac atctgatttt acagaatgga ttattgattt 720 tttggaagtt gagactttaa aaaaaataga tcttacttgc gaaatgcgat ggttgctggg 780 aatacctgaa actgtggatt atattgcttg acttctacct cagaatcttc tttgtttcat 840 gacttaatag tgctttaagt ttggtatatt atttgacctc taggaattct ttgttttaca 900 cagaaataaa aattttaaaa tagaaaatgc ttttactttg taaggtaaga gagtatccat 960 atgcttagat gtgctcgttt ctaaaattct agaggttgat ataatcagct catgaatgca 1020 cagctatgct ttttgtgata gattgtacat aacatcagca gttgaaaggt aaaacaattg 1080 cttttttttt tttttgcatt tgttaagtga ctatggtact ttgtgattcc ttaatctata 1140 gatgagtcag ctccacactt gagtctcttt ttagagggaa atcagtaata aagctgtaaa 1200 ataaggaagg aaaaaaaaaa 1220 50 2020 DNA Homo sapiens misc_feature Incyte ID No 1527017CB1 50 gagaggagtg agtgccgtca ccgagggccg cgccagactg cgacggatac agggagggca 60 agggtttcct tttggcgctt ccctttggac cccggagtga aaaactctaa cgtccagatc 120 agtggagaga aacgcagatt taggaccctg aggagtcttt ttcacccgtt tcccgtcact 180 cgctcaggcg cgccgagggc agtccttgtg gggtcctcgt ggccagccaa gatggttgcc 240 cccgcagtga aggttgcccg aggatggtcg ggcctggcgt tgggcgtgcg gcgggctgtc 300 ttgcagcttc caggggctaa ctcaggtgag atggagccgc tatagtcctg aattcaagga 360 tcccttgatt gacaaggaat attatcgcaa gccagtggag gagctaactg aggaggagaa 420 atatgttcgg gagctcaaga agactcagct catcaaagct gctccagcag gggaaaacaa 480 gttctgtgtt tgaagaccca gtcatcagta aattcaccaa catgatgatg ataggaggaa 540 acaaagtact ggccagatcc ctcatgattc agactctgga agctgtgaaa aggaagcagt 600 ttgagaagta ccatgccgct tctgcagagg aacaggcaac catcgaacgc aacccctaca 660 ccatcttcca tcaagcactg aaaaactgtg agcctatgat tgggctggta cccatcctca 720 agggaggccg tttctaccag gtccctgtac ccctacccga ccggcgtcgc cgcttcctag 780 ccatgaagtg gatgatcact gagtgccggg ataaaaagca ccagcggaca ctgatgccgg 840 agaagctgtc acacaagctg ctggaggctt tccataacca gggccccgtg atcaagagga 900 agcatgactt gcacaagatg gcagaggcca accgtgccct ggcccactac cgctggtggt 960 agagtctcca ggaggagccc agggccctct gccgcaagaa acagtgtgag ctactgccac 1020 gctgaaaact acctgtgggt taaggatgta gttcctttgt aagggtgggc aggcctcgta 1080 agaaagatgt agcagcatat tcactatccg ttaatccttc tttctttgag gctggaactt 1140 gctctctctg cccctatttc cttgtaaaga gggagcacat tgacttggga atttcctcca 1200 ggaaactcag ggctgttttc tcttccctta ggttggggcg gacctttgga catataaagg 1260 aagcagtttt agtatcagaa aagatttatt agaaaattct cacgctgaac tggtgtagca 1320 tgtggtgcag cattcagtga aactggctgg aggaaatagg cttgtttcca gagttgtcct 1380 tatacaaaat gtataaaaag cagtttctgg tgtgacttgt gctctgcctc caccccttga 1440 catcccaaaa tatcccacca gtggctatgc ttacccattt tacagatggg taaactgagg 1500 caccaaggta gtagttgcac taatggttac acagtgcagt ggctcttggg agttgccctt 1560 ctctgcctgg ccgtggtggg ttgtggtggg gaaaggggct cagggcagga ccacggcata 1620 agtgggaaac atctcaccag gagatgggaa agtctagaag ggaagacact caaagtctgg 1680 aagggaaaag tctttgggtg aggcagagac tccactgcca gctttagagg tgggtagaag 1740 aaaggccagt gctggtgagg aaaccctgat ctggaggcta gtcggagact tcgctgtagt 1800 atacttgtgg cactggcgtt gcttccagcc gttggccgtt gttctttccc aagcccgggc 1860 ccgcccccgg gaaacttcca aatgaatttt tcccaaggca aagcnagcna accttggggg 1920 cccaagggga agcttnaaag gncccaattt ttggggaanc caagggnaaa gncccattnc 1980 ccccggggnt ttaaggccnc cnaaaaagaa ggcttccctt 2020 51 637 DNA Homo sapiens misc_feature Incyte ID No 1647264CB1 51 cggccagtgc aagctaaaat taaccctcac taaagggaat aagcttgcgg ccgccgagcc 60 cagctccgcc gccgagcgcc tgtgccggca ccgtacacca tggagcgccc ggataaggcg 120 gcgctgaacg cactgcagcc tcctgagttc agaaatgaaa gctcattagc atctacactg 180 aagacgctcc tgttcttcac agctttaatg atcactgttc ctattgggtt atatttcaca 240 actaaatctt acatatttga aggcgccctt gggatgtcca atagggacag ctatttttac 300 gctgctattg ttgcagtggt cgccgtccat gtggtgctgg ccctctttgt gtatgtggcc 360 tggaatgaag gctcacgaca gtggcgtgaa ggcaaacagg attaaagtga acatcacctt 420 tttatagcat taaattcatt ttttaaaatg ataaatgctg gagggggcca tctgatttga 480 ataaagttga aagaacatgt taaagtcagt cttaaggagt cacgtttgag tatgtaaatt 540 ttgatccttc taatatgttg ggtttgatat tcagttttac tgtatgaatc gattgcaatg 600 agaattggaa aagtagtaca agaatatgta attatta 637 52 717 DNA Homo sapiens misc_feature Incyte ID No 1721989CB1 52 ggctgggcct ggcgcgcagg cgctaggaag aggccgcgtg gggcgaaggc ggcgcttggc 60 tggtggggcc cgcggcggga ttttcccggg cggcgagagc ggatctatct tgggatccca 120 tggctttctt tactgggctc tggggcccct tcacctgtgt aagcagagtg ctgagccatc 180 actgtttcag caccactggg agtctgagtg cgattcagaa gatgacgcgg gtacgagtgg 240 tggacaacag tgccctgggg aacagcccat accatcgggc tcctcgctgc atccatgtct 300 ataagaagaa tggagtgggc aaggtgggcg accagatact actggccatc aagggacaga 360 agaaaaaggc gctcattgtg gggcactgca tgcctggccc ccgaatgacc cccagatttg 420 actccaacaa cgtggtcctc attgaggaca acgggaaccc tgtggggaca cgaattaaga 480 cacccatccc caccagcctg cgcaagcggg aaggcgagta ttccaaggtg ctggccattg 540 ctcagaactt tgtgtgagtt gagcccaggc ctctggttgc aggactcgtg aatggagcag 600 ttctgagaac cacccttttg ctaagggagc ttgggagcca catggctgct cccttcacac 660 tgggtaacag tgtagtatcc tgtgagagaa taaatgtatt catttaaaaa aaaaaaa 717 53 2061 DNA Homo sapiens misc_feature Incyte ID No 1730581CB1 53 ggctcgcaca cacttcggca cgaggaaagg caggaaaggg caggccgggt gagcagacgg 60 atcggccgac tagacagcca accagcaaca acgaactgag ctcgcatact accgcttacg 120 catctaacca accgcccatc tagctaaccc gagcccctcc accgtcaact caggttcggc 180 cggtccccgg cccgcctgcc ggagccgtgg tggcagcccc gggaggagca ctggcgtctg 240 tttccttcga ttctcgggat tcgaagatgg ctgcacagtc agcgccgaaa gttgtgctaa 300 aaagcaccac caagatgtct ctaaatgagc gctttactaa tatgctgaag aacaaacagc 360 cgacgccagt gaatattcgg gcttcgatgc agcaacaaca gcagctagcc agtgccagaa 420 acagaagact ggcccagcag atggagaata gaccctctgt ccaggcagca ttaaaactta 480 agcagaagag cttaaagcag cgcctgggta agagtaacat ccaggcacgg ttaggccgac 540 ccataggggc cctggccagg ggagcaatcg gaggacgagg cctacccata atccagagag 600 gcttgcccag aggaggacta cgtgggggac gtgccaccag aaccctactt aggggcggga 660 tgtcactccg aggtcaaaac ctgctccgag gtggacgagc cgtagctccc cgaatgggct 720 taagaagagg tggtgttcga ggtcgtggag gtcctgggag agggggccta gggcgtggag 780 ctatgggtcg tggcggaatc ggtggtagag gtcggggtat gataggtcgg ggaagagggg 840 gctttggagg ccgaggccga ggccgtggac gagggagagg tgcccttgct cgccctgtat 900 tgaccaagga gcagctggac aaccaattgg atgcatatat gtcgaaaaca aaaggacacc 960 tggatgctga gttggatgcc tacatggcgc agacagatcc cgaaaccaat gattgaagcc 1020 tgcccatcct cccatgagag actcttgtta gtcaacacat ctgtaaataa ccttgagata 1080 acagatgaga agaaatctga ttgatgctgg atggacctat cacaataggc tgtggactta 1140 cttgccacca gcttgtgcat ttagtgtgtt ccttttactt tttgatactg tgttgtatga 1200 aacccttttg tcctttgatt tggttttttg tttttgtttt tttagggggg agggggggtt 1260 tcccctcctt tgcccagact tctctttgaa cacaaatgca ttagccttgt ggctagaaca 1320 ccctcttcct acctctgtct cccctcactt gtcatatgct ctgacatgct aacatttctt 1380 ttgttcatcc ctgttgcccc cacagaaaca tcccagaaaa accggtcagt gttccttcct 1440 ccctgatcct taggtttctg aaatagggtt ctgttacatc ctcttcgata gcctgtttaa 1500 aatgtttaga aggtctggag ctcaaaaatg cgttcttcca cattgataat ttagtaaact 1560 gagaacattg acatcactac agggcagcat aagaggttgc ttacatgtgg tagcagctct 1620 ggtttgattc aagttgctac catgtacatt gacagcacat ataccataac cagcgtgttg 1680 ggttgaattg cactttctac ctttgtatga gatttacaga ctttccttct gggtttgtat 1740 catgaccaga ggggtactat agggttggtt tatactgcaa tatagaggat cagaagccat 1800 ttgatttggt aggtgtgtca gaagggagaa tgatggcaga cgaactgctg gaagaggtca 1860 gaagatagcc atgctaaaat gcaattatat cctcatgttt atcccaaact aatcttggac 1920 ttttccactc attagctttg ttttgccctt gtttcccttg aaggtttaag ttcaaccata 1980 ttctgtcaac tgttcagttt cagtggaatc ttgtatttct ggttcattat aacaaactgt 2040 tcgcttaaaa aaaaaaaaaa a 2061 54 1307 DNA Homo sapiens misc_feature Incyte ID No 1740714CB1 54 gcgctgtgac ctagaatggg cgcatgcgcc gagcggaact ggctggtttg aaaaccatgg 60 cgtgggtacc agcggagtcc gcagtggaag agttgatgcc tcggctattg ccggtagagc 120 cttgcgactt gacggaaggt ttcgatccct cggtaccccc gaggacgcct caggaatacc 180 tgaggcgggt ccagatcgaa gcagctcaat gtccagatgt tgtggtagct caaattgacc 240 caaagaagtt gaaaaggaag caaagtgtga atatttctct ttcaggatgc caacccgccc 300 ctgaaggtta ttccccaaca cttcaatggc aacagcaaca agtggcacag ttttcaactg 360 ttcgacagaa tgtgaacaaa catagaagtc actggaaatc acaacagttg gatagtaatg 420 tgacaatgcc aaaatctgaa gatgaagaag gctggaagaa attttgtctg ggtgaaaagt 480 tatgtgctga cggggctgtt ggaccagcca caaatgaaag tcctggaata gattatgtac 540 aagcaacagt aactagtgtc ttggaatatc tgagtaattg gtttggagaa agagacttta 600 ctccagaatt gggaagatgg ctttatgctt tattggcttg tcttgaaaag cctttgttac 660 ctgaggctca ttcactgatt cggcagcttg caagaaggtg ctctgaagtg aggctcttag 720 tggatagcaa agatgatgag agggttcctg ctttgaattt attaatctgc ttggttagca 780 ggtattttga ccaacgtgat ttagctgatg agccatcttg atgtagctga tctctcaggg 840 atagaagata tttctcatga aggcagccta actctgagga aaacaatgcc aattcaagta 900 cagatttcaa cacatcttca acactatgtg aagggttcac atcttaacct gtgcaattca 960 gattgatact cagaatatgg gttgatttga atatctgaaa tatcaatgga aaatcccact 1020 cagtttttga tgaacagttt gaacagtttt ctgtaatcaa gcagcttgca tagaaattgt 1080 atgatgaaat tttacatagg ttcttggtgc tgttttgttc tttttttgtt ttttgttgtt 1140 ttgttattta cttatataca tataaaattt tattgaaaat atgttttggt tactaaaatt 1200 ttgtttgact cctaacaaaa gacaatggat ggccttagca tcagaattaa aataatctgg 1260 attaaatggc aatgtgttca tagtcagcaa taaaattaaa natttta 1307 55 1357 DNA Homo sapiens misc_feature Incyte ID No 1850596CB1 55 ggggcgcgcg acggcgccag ctcggggcag cggaacccag agaagctgaa ggggcggtag 60 cggcggcgac ggcgacgacg acgactcccg cgcgtgtgcc cagcctcttc ccgccgcagc 120 cgcccttttc ctccctccct tacgtccccg agtgcggcag taccgcctcc ttcccagccg 180 cgcggcttcc tccagacctc tcggcgcggg tgagccctat tcccagaggc aggtggtgct 240 gaccctgtaa cccaaaggag gaaacagctg gctaagctca tcattgttac tggtgggcac 300 catgtccttg aagcttcagg caagcaatgt aaccaacaag aatgacccca agtccatcaa 360 ctctcgagtc ttcattggaa acctcaacac agctctggtg aagaaatcag atgtggagac 420 catcttctct aagtatggcc gtgtggccgg ctgttctgtg cacaagggct atgcctttgt 480 tcagtactcc aatgagcgcc atgcccgggc agctgtgctg ggagagaatg ggcgggtgct 540 ggccgggcag accctggaca tcaacatggc tggagagcct aagcctgaca gacccaaggg 600 gctaaagaga gcagcatctg ccatatacag tggctacatc tttgactatg attactaccg 660 ggacgacttc tacgacaggc tcttcgacta ccggggccgt ctgtcgcccg tgccagtgcc 720 cagggcggtc cctgtgaagc gaccccgggt cacagtccct ttggtccggc gtgtcaaaac 780 taacgtacct gtcaagctct ttgcccgctc cacagctgtc accaccagct cagccaagat 840 caagttaaag agcagtgagc tgcaggccat caagacggag ctgacacaga tcaagtccaa 900 tatcgatgcc ctgctgagcc gcttggagca gatcgctgcg gagcaaaagg ccaatccaga 960 tggcaagaag aagggtgatg gaggtggcgc cggcggcggc ggcggtggtg gtggcagcgg 1020 tggcggtggc agtggtggtg gcggtggcgg tggcagcagc cggccaccag ccccccaaga 1080 gaacacaact tctgaggcag gcctgcccca gggggaagca cggacccgag acgacggcga 1140 tgaggaaggg ctcctgacac acagcgagga agagctggaa cacagccagg acacagacgc 1200 ggatgatggg gccttgcagt aagcagcctg acaggagcaa tggccaccag caggtgaagg 1260 gcatcgctgc cccaggcctc aagccgggca cccaaccctg gatgccaccc cccagcgggt 1320 accagaggaa agctggcagc aggcgcctcc tccccca 1357 56 1749 DNA Homo sapiens misc_feature Incyte ID No 1856109CB1 56 ctggcccgac tactttcgtt ccgtcttcca tcgttttctc tcgtgcaatg gcgtccgggc 60 tggtaagatt gctgcagcag ggacatcgct gcctcctggc tccagtcgcc cccaagctgg 120 tccctccggt tcggggagtg aagaagggat tccgcgccgc cttccgcttc cagaaggagt 180 tagagcggca gcgccttctg cggtgcccgc cgccgcccgt gcgccgttca gagaagccga 240 actgggatta ccatgcagaa atacaagctt ttggacatcg gttacaggaa aacttttcct 300 tagatcttct caaaactgca tttgttaata gctgctatat taaaagtgag gaggccaaac 360 gccaacaact tgggatagag aaagaagctg ttcttctgaa tcttaaaagt aatcaagaac 420 tatccgaaca agggacatct ttttcacaga cttgccttac acagtttctt gaagacgagt 480 acccagacat gcccactgaa ggcataaaaa atcttgttga ctttctcact ggtgaggaag 540 tcgtgtgtca cgtggctaga aacttggctg tggagcagtt aacactgagt gaagaattcc 600 cagtgccccc agctgtgtta cagcagactt tctttgcagt tattggagcc ctgttacaga 660 gcagtggacc tgagaggact gcacttttca tcagggactt cttaattact caaatgactg 720 gaaaagagct ctttgagatg tggaagataa taaatcccat ggggctattg gtagaagaac 780 tgaagaaaag gaatgtttca gctcctgaat caagacttac taggcagtct ggtggcacca 840 cagctttgcc tttgtatttt gttggcttat actgtgataa aaagttgatt gcagaaggac 900 ctggggaaac agtattggtt gcagaagaag aggctgctcg agtggccctt agaaaacttt 960 atggattcac agaaaataga cggccgtgga actattccaa gcccaaagaa accttgagag 1020 cagaaaagag catcactgcc agctagccgc catggatgca gcagcctgaa acttgagagc 1080 gaaagtgaga taaatgtcaa aggtgtttca agccagacat tttcacaatt gtgaagaaat 1140 agatgttttg tttctgtttt ttactgtgtt cccaaaatta aataaatgtt aaccaagtca 1200 cagtgttttt ggttttgttt ttctgaaatc ttggtttgat caaatctttt tttttttctc 1260 ttgagatgga gtcttactct gtcgcccagg ctggactgca gtggtgcgat ctcggctcac 1320 tgcaacctcc acctcacagg ttcaagcgat tctcgtggct cagcctccct agtagctggg 1380 attacaggca cacaccacca tacctggcta atttttgtat ttttggtaga gatggggttt 1440 caccaagttg gctagactag tcttgaactc ctgacctcag gtgatccacc cgccttggcc 1500 tcccaaagtg ctgggattac aggtgtgagc cactataccc gaccagatca aatctttttt 1560 tgacattttt gcaaaaaaat tttcctaatg ttcttgattt aattgtatag aatttgtata 1620 attaggtgta ttttatttgc ctctagcttt gaggtatcat aatttatgta tcttatgtga 1680 attttttgct gtaataccaa taaagttttt tttctccaca tgttaaaaaa aaaaaaaaaa 1740 aaaaaaaaa 1749 57 991 DNA Homo sapiens misc_feature Incyte ID No 1921719CB1 57 cgaaagatgg cggcgcccgt aaggcggacg ctgttagggg tggcgggggg ttggcggcgg 60 ttcgagaggc tctgggccgg cagtctaagc tctcgcagcc tggctcttgc agccgcaccc 120 tcaagcaacg gatccccatg gcgcttgttg ggcgcgttgt gcctgcagcg gccacctgta 180 gtctccaagc cgttgacccc attgcaggaa gagatggcgt ctctactgca gcagattgag 240 atagagagaa gcctgtattc agaccacgag cttcgtgctc tggatgaaaa ccagcgactg 300 gcaaagaaga aagctgacct tcatgatgaa gaagatgaac aggatatatt gctggcgcaa 360 gatttggaag atatgtggga gcagaaattt ctacagttca aacttggagc tcgcataaca 420 gaagctgatg aaaagaatga ccgaacatcc ctgaacagga agctagacag gaaccttgtc 480 ctgttagtca gagagaagtt tggagaccag gatgtttgga tactgcccca ggcagagtgg 540 cagcctgggg agacccttcg aggaacagct gaacgaaccc tggccacact ctcagaaaac 600 aacatggaag ccaagttcct aggaaatgca ccctgtgggc actacacatt caagttcccc 660 caggcaatgc ggacagagag taacctcgga gccaaggtgt tcttcttcaa agcactgcta 720 ttaactggag acttttccca ggctgggaat aagggccatc atgtgtgggt cactaaggat 780 gagctgggtg actatttgaa accaaaatac ctggcccaag ttaggaggtt tgtttcagac 840 ctctgatggg ccgagctgcc tgtggacggt gctcagacaa gtctgggatt agagcctcaa 900 ggacattgtg tgattgcctc acatttgcag gtaatatcaa gcagcaaact aaattctgag 960 aaataaacga gtctattact gaaaaaaaaa a 991 58 1188 DNA Homo sapiens misc_feature Incyte ID No 2099829CB1 58 ccgtcttccg ccgcacgtgg attcagcgcg atgcccaaat ccaagcgcga caagaaagtc 60 tccttaacca aaactgccaa gaaaggcttg gaattgaaac aaaacctgat agaagagctt 120 cggaaatgtg tggacaccta caagtacctt ttcatcttct ctgtggccaa catgaggaac 180 agcaagctga aggacatccg gaacgcctgg aagcacagcc ggatgttctt tggcaaaaac 240 aaggtgatga tggtggcctt gggtcggagc ccatctgatg aatacaaaga caacctgcac 300 caggtcagca aaaggttgag gggtgaggtg ggtctcctgt tcaccaaccg cacaaaggag 360 gaggtgaatg agtggttcac gaaatacaca gaaatggact acgcccgagc tggtaacaaa 420 gcagctttca ctgtgagcct ggatccaggg cccctggagc agttccccca ctccatggag 480 ccacagctca ggcagctggg cctgcccacc gccctcaaga gaggtgtggt gactctgctg 540 tctgactacg aggtgtgcaa ggagggcgat gtgctgaccc cagagcaggc tcgcgtcctg 600 aagctttttg ggtatgagat ggctgaattc aaggtgacca tcaaatacat gtgggattca 660 cagtcgggaa ggttccagca gatgggagac gacttgccag agagcgcatc tgagtccaca 720 gaagagtcag actcagaaga tgatgactga aagggactcg ggactgaagg tctcctggaa 780 gcttctgggt ctcactggac catcaggact gctgccgccc ctctggagag agcagctttt 840 tatttgtctg tagacaggga acatgatggg cactgacctc ctgtaaagaa taaaactgtg 900 ggccgggcgc ggtggctcac gcctggaatc ccagcacttt gggaagccga ggtgggcaga 960 tcataaggtc aggagattaa gaccatcctg gctaacacgg tgaaaccccg tctctactaa 1020 aaatagaaaa aaaaactagt tgggcatagt ggcatgtgcc tgtagtccca gctactcagg 1080 aggctgaggc aggagaatca cttgaacccg ggaggtggag gttgccgtga gttgagattg 1140 gaccactgct ctccagcctg ggcaacagag taaaactctg tcccaaaa 1188 59 1454 DNA Homo sapiens misc_feature Incyte ID No 2416915CB1 59 gttgtcactc tctcgggttg ttactctgta gcttcccggc tcgcgaaagg gaggacctgt 60 ctgggtcatg gattttgaga atcttttctc aaaacccccc aacccggccc tcggcaaaac 120 ggccacggac tctgacgaaa gaatcgatga tgaaatagat acagaagttg aagaaacaca 180 agaagagaaa attaaactgg agtgcgagca aattcccaaa aaatttagac actctgcaat 240 atcaccaaaa agttcgctgc atagaaaatc aagaagtaag gactatgatg tatatagtga 300 taatgatatc tgcagtcagg aatcagaaga taattttgcc aaagagcttc aacagtacat 360 acaagccaga gaaatggcaa atgctgctca acctgaagaa tctacaaaga aagaaggagt 420 aaaagatacc ccacaggctg ctaaacaaaa aaataaaaat cttaaagctg gtcacaagaa 480 tggcaaacag aagaaaatga agcgaaaatg gcctggccct ggaaacaaag gatcaaatgc 540 tttgctgagg aacagcggct cacaggaaga ggatggtaaa cctaaagaga agcagcagca 600 tttgagtcag gcattcatca accaacatac agtggaacgc aagggaaaac aaatttgtaa 660 atattttctt gaaaggaaat gtattaaggg agaccagtgt aaatttgatc atgatgcaga 720 gatagaaaaa aaaaaggaaa tgtgtaagtt ttatgtacaa ggatattgta ccagaggtga 780 aaactgtctg tatttgcata atgaatatcc ttgtaagttt taccatacag gaacaaaatg 840 ttatcaggga gaatactgca agttttctca tgctccactg actcctgaaa cacaagaatt 900 gttggctaaa gttttggata ctgaaaagaa gtcatgtaaa taaaatagac ataaaaaggt 960 agcaatgtac agataaagag tactttaacg cccatgcgtg ttcaagactg ttcaagactg 1020 gtgatttgga gtagtttaca agattcctca ttcagagtgc cctcttgtgt gactggggtg 1080 atgtgcagct tccataatgg atgggacaga gagctgggat ctaatgtaca agtgaagggc 1140 ttggtcttcc ctgagacatt ccagccattg gaataggaga ggagcatata tggcagaggt 1200 gatggctggt gggtaaatgt gatagtaaat tgtagaaacc tcttctgatt gattggattt 1260 ccttaataaa atcggaagca aggttaggct gagtgagggt gagtaaagag gtagaggagg 1320 tttgaggaga gagaactgct cggaagacat tggtagatgg accataaaaa cagagttagt 1380 tctctttatg acattaaata gttttacaac atatttttaa tggttcacaa tttcatttta 1440 gggcttaaaa taaa 1454 60 1588 DNA Homo sapiens misc_feature Incyte ID No 2472784CB1 60 cccggacgaa gggggagagt agacagcaga accagcggcg gcggctaagc agagactgta 60 gtagcggcga cagcgacgac ggcagcgatg gctggggcgg ggccagcccc gggactcccg 120 ggtgcaggag gacccgtggt cccgggtcct ggcgctggca tcccgggcaa aagcggcgag 180 gaacgcttga aggaaatgga ggcggagatg gccctgtttg agcaggaagt tctgggggct 240 ccagtacctg gaatcccaac tgctgtgcct gcggtgccca ctgtccccac ggtccccaca 300 gtagaagcga tgcaggtccc agcggctcct gtgatccgcc caattatcgc gaccaacaca 360 taccagcagg tccagcagac tctggaggcc cgagcagctg ctgcagccac agtagttcct 420 cccatggtgg gtggccctcc ttttgtaggc cctgttggct ttggccctgg tgatcggagt 480 cacctggaca gcccagaggc tcgagaagcc atgttcctgc ggcgggcagc agccgtcccc 540 cgccctatgg ccctaccgcc ccctcaccag gccctcgtgg gcccccctct gcctgggccc 600 cctggaccac ccatgatgct gccaccaatg gctcgggctc cagggccccc gctgggctcc 660 atggctgcac tgaggccccc tctggaagag ccagcagcac cccgagagct gggcctaggc 720 ctggggttgg gcctgaaaga gaaggaagag gcagtggtgg cggcggcggc tgggctggag 780 gaggctagcg cggctgtggc cgtgggggca ggaggtgccc cagctggccc tgcagtcatt 840 gggcccagcc tgccgctggc cctggccatg ccattgcccg agcctgagcc cctgcccctc 900 ccgttggagg tcgtccgcgg cctcctgccc ccgctgcgca ttcctgaact cctgtccctg 960 cgtcctcggc cccggccccc tcggccagag ccacccccag gcctcatggc tcttgaggtc 1020 ccagagcccc tgggtgaaga caagaagaag gggaagccag agaaattgaa acggtgcatt 1080 cgcacagcgg cagggagcag ctgggaggac cccagcctgc tggagtggga tgcagatgac 1140 ttccggatct tctgtgggga tctgggcaat gaggtgaacg atgacatctt ggcacgcgcc 1200 ttcagccgct tcccatcctt ccttaaggcc aaggtgatcc gtgacaagcg cacaggcaag 1260 accaagggct acggcttcgt cagcttcaag gaccccagcg actacgtgcg cgccatgcgt 1320 gagatgaatg ggaagtatgt gggctcgcgc cccatcaagc ttcgcaagag catgtggaag 1380 gaccggaatc tggacgtggt ccgcaagaag cagaaggaaa agaagaagct gggcctgaga 1440 tagggtctgt ggccaggcac ccgctcccac ctggccgggc gctggctcct ccctcagttc 1500 tctttggaaa acccccagct gtccacccat cccctgcccc aaaaccagtt tcaataaatt 1560 tacgttcatt tccaaaaaaa aaaaaaaa 1588 61 2111 DNA Homo sapiens misc_feature Incyte ID No 2598981CB1 61 cgcaggcggg cctcgcgggt ccgggagcgc ggcggagacg atgcctgaga tcagagtcac 60 gcccttgggg gccggccagg acgtgggccg aagctgcatc ctggtctcca ttgcgggcaa 120 gaatgtcatg ctggactgtg gaatgcacat gggcttcaat gacgaccgac gcttccctga 180 cttctcctac atcacccaga acggccgcct aacagacttc ctggactgtg tgatcattag 240 ccacttccac ctggaccact gcggggcact cccctacttc agcgagatgg tgggctacga 300 cgggcccatc tacatgactc accccaccca ggccatctgc cccatcttgc tggaggacta 360 ccgcaagatc gccgtagaca agaagggcga ggccaacttc ttcacctccc agatgatcaa 420 agactgcatg aagaaggtgg tggctgtcca cctccaccag acggtccagg tagatgatga 480 gctggagatc aaggcctact atgcaggcca cgtgctgggg gcagccatgt tccagattaa 540 agtgggctca gagtctgtgg tctacacggg tgattataac atgaccccag accgacactt 600 aggagctgcc tggattgaca agtgccgccc caacctgctc atcacagagt ccacgtacgc 660 cacgaccatc cgtgactcca agcgctgccg ggagcgagac ttcctgaaga aagtccacga 720 gaccgtggag cgtggtggga aggtgctgat acctgtgttc gcgctgggcc gcgcccagga 780 gctctgcatc ctcctggaga ccttctggga gcgcatgaac ctgaaggtgc ccatctactt 840 ctccacgggg ctgaccgaga aggccaacca ctactacaag ctgttcatcc cctggaccaa 900 ccagaagatc cgcaagactt ttgtgcagag gaacatgttt gagttcaagc acatcaaggc 960 cttcgaccgg gcttttgctg acaacccagg accgatggtt gtgtttgcca cgccaggaat 1020 gctgcacgct gggcagtccc tgcagatctt ccggaaatgg gccggaaacg aaaagaacat 1080 ggtcatcatg cccggctact gcgtgcaggg caccgtcggc cacaagatcc tcagcgggca 1140 gcggaagctc gagatggagg ggcggcaggt gctggaggtc aagatgcagg tggagtacat 1200 gtcattcagc gcacacgcgg acgccaaggg catcatgcag ctggtgggcc aggcagagcc 1260 ggagagcgtg ctgctggtgc atggcgaggc caagaagatg gagttcctga agcagaagat 1320 cgagcaggag ctccgggtca actgctacat gccggccaat ggcgagacgg tgacgctgcc 1380 cacaagcccc agcatccccg taggcatctc gctggggctg ctgaagcggg agatggcgca 1440 ggggctgctc cctgaggcca agaagcctcg gctcctgcac ggcaccctga tcatgaagga 1500 cagcaacttc cggctggtgt cctcagagca agccctcaaa gagctgggtc tggctgagca 1560 ccagctgcgc ttcacctgcc gcgtgcacct gcatgacaca cgcaaggagc aggagacggc 1620 attgcgcgtc tacagccacc tcaagagcgt cctgaaggac cactgtgtgc agcacctccc 1680 ggacggctct gtgactgtgg agtccgtcct cctccaggcc gccgcccctt ctgaggaccc 1740 aggcaccaag gtgctgctgg tctcctggac ctaccaggac gaggagctgg ggagcttcct 1800 cacatctctg ctgaagaagg gcctccccca ggcccccagc tgaggccggc aactcaccca 1860 gccgccacct ctgccctctc ccagctggac agaccctggg cctgcacttc aggactgtgg 1920 gtgccctggg tgaacagacc ctgcaggtcc catccctggg gacagaggcc ttgtgtcacc 1980 tgcctgccca ggcagctgtt tgcagctgaa gaaacaaact ggtctccagg ctgtcttgcc 2040 tttattcctg gttagggcag gtggtcctag acagcagttt ccagtaaaag ctgaacaaaa 2100 gaaaaaaaaa a 2111 62 1155 DNA Homo sapiens misc_feature Incyte ID No 2738075CB1 62 cccacgcgtc cgcccacgcg tccgcccacg cgtccggccg ggaagaagca ccgtggctgc 60 tattatctgc tctccgcgcc tgacccctcc caggactcgt gatgccaagg ccgctgcgag 120 cggctacgaa gagtcggggt tgagccccag ctgagccgag ggctcgcact cttctggtct 180 cccaggccca acccacctga agaaatgagt ggtggattgg ctccaagtaa gagcacagtg 240 tatgtatcca acttgccttt ttccctgaca aacaatgact tgtaccggat attttccaag 300 tatggcaaag ttgtaaaggt taccatcatg aaagataaag ataccaggaa gagtaaaggg 360 gttgcattta ttttattttt ggataaagac tctgcacaaa actgtaccag ggcaataaac 420 aacaaacagt tatttggtag agtgataaaa gcaagcattg ctattgacaa tggaagagca 480 gctgagttca tccgaaggcg aaactacttt gataaatcta agtgttatga atgtggggaa 540 agtggacact taagttatgc ctgtccgaaa aatatgctcg gagaacgtga gcctccaaag 600 aagaaagaaa aaaagaaaaa aaagaaagct cctgaaccag aagaagaaat tgaggaagta 660 gaagaaagtg aagatgaagg ggaggatcct gctcttgaca gcctcagtca ggccatagca 720 ttccagcaag ccaaaattga agaagaacaa aaaaaatgga aacccagttc aggagtcccc 780 tcaacatcag atgattcaag acgcccaagg ataaagaaaa gcacatattt cagtgatgag 840 gaagaactta gtgattaaaa tcttgcccca gcacagtaat aaaaatcaag atttgttagt 900 aacaatcttg aagagctaat tttaataaaa ataagaaaaa ttaatactat catgttaata 960 ctattattgt catcccaaga aaaaagatat tttaaaaatt tatttgaaaa gttcattata 1020 agggctttat tcatgcctga tttgtttaca tgaggacttc tgaaattaat ccttaaaaca 1080 aacttcctga agaccgaaaa gttgaatgat ttattgttac ttatattaat aaacttttca 1140 agagaaaaan nnnnn 1155 63 1673 DNA Homo sapiens misc_feature Incyte ID No 2279049CB1 63 gttttgggtc gcagtatgct agaattttga ggctcccttc tgatgaaaat tgagctgtcc 60 atgcagccat ggaacccggg ttacagcagt gagggggcca cggctcaaga aacttacaca 120 tgtccaaaaa tgattgagat ggagcaggcg gaggcccagc ttgctgagtt agacctgcta 180 gccagtatgt tccctggtga gaatgagctc atagtgaatg accagctggc tgtagcagaa 240 ctgaaagatt gtattgaaaa gaagacaatg gaggggcgat cttcaaaagt ctactttact 300 atcaatatga acctggatgt atctgacgaa aaaatggcga tgttttctct ggcctgtatt 360 cttcccttta aatacccggc agttctgcct gaaattactg tcagatcagt attattgagt 420 agatcccagc agactcagct gaacacagat ctgactgcat tcctgcaaaa acattgtcat 480 ggagatgttt gtatactgaa tgccacagag tgggttagag aacacgcctc tggctatgtc 540 agcagagata cttcatcttc acccaccaca ggaagcacag tccagtcagt tgacctcatc 600 ttcacgagac tctggatcta cagccatcat atctataaca aatgcaaaag aaagaatatt 660 ctagagtggg caaaggagct ttccctgtct gggtttagca tgcctggaaa acctggtgtt 720 gtttgtgtgg aaggcccaca aagtgcctgt gaagaattct ggtcaagact cagaaaatta 780 aactggaaga gaattttaat tcgccatcga gaagacattc cttttgatgg tacaaatgat 840 gaaacggaaa gacaaaggaa attttccatt tttgaagaaa aagtgttcag tgttaatgga 900 gccaggggaa accacatgga ctttggtcag ctctatcagt tcttaaacac caaaggatgt 960 ggggatgttt tccagatgtt ctttggtgta gaaggacaat gacatcaaga gtagttgaaa 1020 gtatcttgcc actgttggcc ttttgatttt tttttcccac tttttcttga aagattaagt 1080 aattttattt tagttccatt ctagaatgtt ggggagtggg gcacaagaaa aaatagtata 1140 gctgaaatgc atctgttaaa aatgtcatga ttgaaagcag aactgagttt caaattacaa 1200 ccttaaaatt gttgttagat atttcttcac atatcagctg cccattttga aaaagaaatt 1260 atccataaag gtaatgttgg tgctccaatt tgccagccat tcccaacccc cttctccctt 1320 acctgccttc actaaagaac ccagaaaagc taattgctcc cctttcagcc tctgttgcaa 1380 ctaacaactc tcagtggcct caggacacag ctttggcctt gggaattctg ggaaaacttt 1440 tacttcctga ttaaagatac atatgcagct aggccacctc ctccccccct tactgccata 1500 aacaccaaag tgatgactgg agctggagga gttatttgaa ccacgacgaa gggccaagag 1560 aaccacgaag atgccagttg ccacattgtt gagctgctga cccaacacca gccattgcct 1620 gtctctaaac atcttatgaa ataaaaccag ttttgtttaa aaaaaaaaaa aaa 1673 64 584 DNA Homo sapiens misc_feature Incyte ID No 2660904CB1 64 aaaataaggc atttgggatg ccgatgttaa aaggagaagg taatcagaga agaaaaaagg 60 aagtcggtgg agagttctgc gaagattttg aagatttcta gagaagcagg gggttctgga 120 gaagggaata gacttggcca gatacccagg aagacttcct caacagatgt cccatcatgc 180 tgagattcaa cgcgacattt tagagtcatg caaccatgtg agaaaaaaag tcccagtaac 240 ctttgttggg gctggagggc aggatcccga ggtcccggag gagctgctcc acctcctcca 300 gccaggacag cgcgtgcctc aggacgtcca gcaccacctt ctggagcccc gagacaggtg 360 ggctcacctg gaggtgctga agaaggtcga cctccttctt caggtcatgg ctgcaacagg 420 atattttcat gcaagcctgc aaagaggtga gatcatgagg agcccaggcc ctgtggccag 480 aaatagcccc tgacgtgacc ttcgaggaac agcgttcttg actctgccac gaagcaggca 540 gcgccacgta ttggccgcct tgggaggact cagttttttt cttt 584 65 978 DNA Homo sapiens misc_feature Incyte ID No 3179424CB1 65 ccggctacct gttggtgtgt atgcagagca tccctgtgcc ccgcggatat agactggcgc 60 gcctctgttg cgcaggcgca gaactacaac ttcagggttt tccccaacgg cctctttttt 120 gcacgttagg agaaactaca tttcccataa tcctttgttc cagggctgga gcggctctgg 180 gctccggaat cgcccgcagc cggtactgcg ggacccactg cggatatggc tgtcttggct 240 ggatccctgt tgggccccac gagtaggtcg gcagcgttgc tgggtggcag gtggctccag 300 ccccgggcct ggctggggtt cccagacgcc tggggcctcc ccaccccgca gcaggcccgg 360 ggcaaggctc gcgggaatga gtatcagccg agcaacatca aacgcaagaa caagcacggc 420 tgggtccggc gcctgagcac gccggccggc gtgcaggtca tccttcgccg aatgctcaag 480 ggccgcaagt cgctgagcca ttgaggatcg cgacgcagtc ggcgggaccc tcatggaagc 540 atcgccctcg cctcggacct tgcctggcgc tatttttgca gggagctggg gagcaggaac 600 gcctcggacc tgagtgctct ccatattgtg gggttgaagt ctggatggga gcttgccaag 660 tcccttttta ggctttttaa ttaggaagca tttcgaacct gcgcaacaga ccaaagaaca 720 gtacaaagaa catccgtgta cccagtaccc tgactaccga ctacctacaa cccgtccctg 780 ccccatcctg agttcttttg aagctgatct caggcatcgg attatttctt ctgtaaatat 840 ttcagaatgt atctctccaa gatgagagct cattaaaaga caattacaaa gcttatcaca 900 tccaaaagaa ttatcaataa ttttgaaata ttattaaacg tgtaataaat gttcaaagtt 960 ccacttgcaa aaaaaaaa 978 66 1055 DNA Homo sapiens misc_feature Incyte ID No 2885096CB1 66 cagcctcaga gatggatgga tctgcaatgc catggctggg ggtgttccag ggcagcctgc 60 aggggtgggg ctggcactga ttgcaactga cagccaggag accaggcctg ggagggcagg 120 cccagggtca ggggagagcc tgagtgcttc ccacctcttc atctcagact ttgcatactg 180 ctgggaaaac tttgtgtgca atgaaggtca gccattcatg ccttggtaca aattcgatga 240 caattatgca tccctgcacc gcacgctaaa ggagattctc agaaacccga tggaggcaat 300 gtacccacac atattctact tccactttaa aaacctactg aaagcctgtg gtcggaacga 360 aagctggctg tgcttcacca tggaagttac aaagcaccac tcagctgtct tccggaagaa 420 gggcgtcttc cgaaaccagg tggatcctga gacccattgt catgcagaaa ggtgcttcct 480 ctcttggttc tgtgacgaca tactgtctcc taacacaaac tacgaggtca cctggtacac 540 atcttggagc ccttgcccag agtgtgcagg ggaggtggcc gagttcctgg ccaggcacag 600 caacgtgaat ctcaccatct tcaccgcccg cctctgctac ttctgggata cagattacca 660 ggaggggctc tgcagcctga gtcaggaagg ggcctccgtg aagatcatgg gctacaaaga 720 ttttgtatct tgttggaaaa actttgtgta cagtgatgat gagccattca agccttggaa 780 gggactacaa accaactttc gacttctgaa aagaaggcta cgggagattc tccagtgagg 840 ggtctccctg ggcctcatgg tctgtctctt ctagcctcct gctcatgctg cacgggcctc 900 ccctccatcc tgcaccagct gtgcttttgc ctggtcatcc tgagcccctc ctggcctcag 960 ggccattcca tagtgccccc ctgcctcacc acctactctc cgctctccca ggttcttcct 1020 gcagaggcct ctttctgcct ccatggctat ccatc 1055 67 2220 DNA Homo sapiens misc_feature Incyte ID No 2901076CB1 67 cggctccgtc gctgacgcgt cgtagacgtt ggggagcggg aaggcaacgg cagcgggatc 60 gggatgaaca gcggcggcgg cttcggtttg ggcttaggct tcggcctcac ccccacgtcg 120 gtgattcagg tgacgaatct gtcgtcggcg gtgaccagcg agcagatgcg gacgcttttt 180 tccttcctag gagaaatcga ggagctgcgg ctctaccccc cggacaacgc acctcttgct 240 ttttcctcca aagtatgtta tgttaagttt cgtgatccat caagtgttgg cgtggcccag 300 catctaacta acacggtttt tattgacaga gctctgatag ttgttccttg tgcagaaggt 360 aaaatcccag aggaatccaa agccctctct ttattggctc ctgctccaac catgacaagt 420 ctgatgcctg gtgcaggatt gcttccaata ccgaccccaa atcctttgac tactcttggt 480 gtttcactta gcagtttggg agctatacca gcagcagcac tagaccccaa cattgcaaca 540 cttggagaga taccacagcc accacttatg ggaaacgtgg atccttccaa aatagatgaa 600 attaggagaa cggtttatgt tggaaatctg aattcccaga caacgacagc tgatcaacta 660 cttgaatttt ttaaacaagt tggagaagtg aagtttgtgc ggatggcagg tgatgagact 720 cagccaactc ggtttgcttt tgtggaattt gcagaccaaa attctgtacc aagggccctt 780 gcttttaatg gagttatgtt tggagacagg ccactgaaaa taaatcactc caacaatgca 840 atagtaaaac cccctgagat gacacctcag gctgcagcta aggagttaga agaagtaatg 900 aagcgagtac gagaagctca gtcatttatc tcagcagcta ttgaaccaga gtctggaaag 960 agcaatgaaa gaaaaggcgg tcgatctcgt tcccatactc gctcaaaatc caggtctagc 1020 tcaaaatccc attctagaag gaaaagatca caatcaaaac acaggagtag atcccataat 1080 agatcacgtt caagacagaa agacagacgt agatctaaga gcccacataa aaaacgctct 1140 aaatcaaggg agagacggaa gtcaaggagt cgttcgcatt cacgggacaa gagaaaagac 1200 actcgagaaa agatcaagga aaaggaaaga gtgaaagaga aagacaggga aaaggagaga 1260 gagagggaaa aggaacgtga aaaagaaaag gaacggggta aaaacaaaga ccgggacaag 1320 gaacgggaaa aggaccggga aaaagacaag gaaaaggaca gagagagaga acgggaaaaa 1380 gagcatgaga aggatcgaga caaagagaag gaaaaggaac aggacaaaga aaaggaacga 1440 gaaaaagaca gatccaaaga gatagatgaa aaaagaaaga aggataaaaa atccagaaca 1500 ccacccagga gttacaatgc atcgcgaaga tctcgtagtt ccagcaggga aaggcgtagg 1560 aggaggagca ggagttcttc cagatcgcca agaacatcaa aaaccataaa aaggaaatct 1620 tctagatctc cgtcccccag gagcagaaat aagaaggata aaaagagaga aaaagaaagg 1680 gaccacatca gtgaaagaag agagagagaa cgttcaacgt ctatgagaaa gagttctaat 1740 gatagagatg ggaaggagaa gttggagaag aacagtactt cacttaaaga gaaagagcac 1800 aataaagaac cagattcaag tgtgagcaaa gaagtagatg acaaggatgc accaaggact 1860 gaggaaaaca aaatacagca caatgggaat tgtcagctga atgaagaaaa cctctctacc 1920 aaaacagaag cagtatagga ccgacaagtg tacctctgca ctcaatgctg gaatcaaatc 1980 caaagctttt aattctctca acaagatgta aacaggaaag aaatctagtt gagcatgaag 2040 ataggatcta acagcttttc cagttgttag atgactttgt ggccatcttg ttattgagta 2100 agaaaataaa gcatggacat catgaaaata acagatgtta cccaaactca tcttctaaaa 2160 tctgtgcatt tccatggtgg ctgacacact tgtcatgtgg tctgttagtg tttgccaaga 2220 68 1890 DNA Homo sapiens misc_feature Incyte ID No 3074572CB1 68 ggcggtgccc ggccggggcc acgccttttc cggcccgcag cgcggcctgg gctcccgcgt 60 gtttaaaagt gcgcttgtgg ctgctgctgt cttaactcct gtgcttggcg gacagacagg 120 cgagatggcg gcggaggtgt tgccgagtgc gaggtggcag tattgtgggg cgcccgacgg 180 gagccagaga gctgtactgg tccagttctc caacgggaag ctacagagtc caggcaacat 240 gcgctttacc ttgtatgaga acaaagattc caccaacccc aggaagagga atcaacggat 300 cctggcagct gaaacagata ggctctccta tgtgggaaac aattttggga ctggagccct 360 caaatgcaac actttgtgca ggcactttgt gggaattttg aacaagacct ctggccaaat 420 ggaagtatat gatgctgaat tgttcaatat gcagccacta ttttcagatg tatcagttga 480 gagtgaactg gcgctagaga gtcagaccaa aacttacaga gaaaagatgg attcttgtat 540 tgaagccttt ggtaccacca aacagaagcg agctctgaac accaggagaa tgaacagagt 600 tggcaatgaa tctttgaatc gtgcagtggc taaagctgca gagactatca ttgatacgaa 660 gggtgtgact gctctggtca gcgatgctat ccacaatgac ttgcaagatg actccctcta 720 ccttcctccc tgctatgatg atgcagccaa gcctgaagac gtgtataaat ttgaagatct 780 tctttcccct gcggagtatg aagctcttca gagcccatct gaagctttca ggaacgtcac 840 gtcagaagaa atactgaaga tgattgagga gaacagccat tgcacctttg tcatagaagc 900 gttgaagtct ttgccatcag atgtggagag ccgagaccgc caggcccgat gcatatggtt 960 tctggatacc ctcatcaaat ttcgagctca tagggtagtt aagcggaaaa gtgctctggg 1020 acctggagtt ccccacatca tcaacaccaa actgctgaag cactttactt gcttgaccta 1080 caacaatggc agattacgga acttaatttc ggattctatg aaggcgaaga ttactgcata 1140 tgtgatcata cttgccttgc acatacatga cttccaaatt gacctgacag tgttacagag 1200 ggacttgaag ctcagtgaga aaaggatgat ggagatagcc aaagccatga ggctgaagat 1260 ctccaaaaga agggtgtctg tggccgccgg cagtgaagaa gatcacaaac tgggcaccct 1320 gtccctcccg ctgcctccag cccagacctc agaccgcctg gcaaagcgga ggaagattac 1380 ctagacgcat gctttccaga cagggcgttt tggctgcatc acagccactg gctggtccta 1440 ttcatttcca tttttatgta tgttttgaaa agaaaaggtc cggggatggt ggctcacacc 1500 tgaaatccca gcactttggg aggccgaggc aggaagatca ttgagctcag gagtttgaaa 1560 ccagtctgga caacataggg agaccccatc tctaccggag gaaaaaaaaa agagtcaggc 1620 ctggtggtgt gcgcctgtaa tcccagctac tcgggaggct gaggcaggac gattacttga 1680 gcttgggaaa tcaaggttgc agtgagctat gattgtgtgg ccacactcca tcctgggtca 1740 cagagtgaga ccttgtctca aaaaaagtaa cataaggaaa aaagaagcct tgctttagca 1800 caggtatgaa gccagaagcc agcatctcaa ctgtgcttgt cttatgcaga aatataaagc 1860 gatggccagg ttggacttca aaaaaaaaaa 1890 69 2893 DNA Homo sapiens misc_feature Incyte ID No 1437895CB1 69 aattgggctc accaggatcg tccaggataa tcttccaatc tcaagtgtgg tttattgaca 60 atcatttaca atgccgaaga gtgctgtagt gagccagcac agtgggtaac acagcaacgg 120 agaacagatg caggtttgag gaatttaact tgctaaaacc ttgaactgaa gtcttagaga 180 ttggaacata cgggtttgta taaataggct tttaagccct gtttgcaatg ggttactgat 240 aggagaaact tgcttgtgga atgtcagctg cgtgagctca ctgtcagaca agatggaaga 300 agaagggctg gagtgtccaa actcttcctc tgaaaaacgc tattttcctg aatccctgga 360 ttccagcgat ggggatgagg aagaggtttt ggcctgtgag gatttggaac ttaacccctt 420 tgatggattg ccatattcat cacgttatta taaacttctg aaagaaagag aagatcttcc 480 tatatggaaa gaaaaatact cctttatgga gaacctgctt caaaatcaaa tcgtgattgt 540 ttcaggagat gctaaatgtg gtaagagcgc tcaggttcct cagtggtgtg ctgaatattg 600 tctttccatc cactaccagc acgggggcgt gatatgcaca caggtccaca agcagactgt 660 ggtccagctc gccctgcggg tggcggatga aatggatgtt aacattggtc atgaggttgg 720 ctacgtgatc cctttcgaga actgctgtac caacgaaaca atcctgaggt attgtactga 780 tgatatgctg caaagagaaa tgatgtccaa tccttttttg ggtagctatg gggtcatcat 840 cttagatgat attcatgaaa gaagcattgc aactgatgtg ttacttggac ttcttaaaga 900 tgttttacta gcaagaccag aactgaagct cataattaac tcctcacctc acctgatcag 960 caaactcaat tcttattatg gaaacgtgcc tgtcatagaa gtgaaaaata aacaccctgt 1020 ggaggttgtg taccttagtg aggctcaaaa ggattctttt gagtctattt tacgccttat 1080 ctttgaaatt caccactcgg gtgagaaagg tgacattgta gtctttctgg cctgtgaaca 1140 agatattgag aaagtctgtg aaactgtcta tcaaggatct aacctaaacc cagatcttgg 1200 agaactggtg gttgttcctt tgtatccaaa agagaaatgt tcattgttca agccactcga 1260 tgaaacagaa aaaagatgcc aagtttatca aagaagagtg gtgttaacta ctagctctgg 1320 agagtttttg atctggagca actcagtcag atttgttatc gatgtgggtg tggaaagaag 1380 aaaggtgtac aacccgagaa taagagcaaa ctcgctcgtc atgcagccca tcagccagag 1440 ccaggcagag atacgcaagc agattcttgg ctcatcttct tcaggaaaat ttttctgcct 1500 gtacactgaa gaatttgcct ccaaagacat gacgccactg aagccagcag aaatgcagga 1560 agccaaccta acaagcatgg tgctttttat gaagaggata gacattgcgg gcctaggcca 1620 ctgtgacttc atgaacagac cagcaccaga aagtttgatg caggcattgg aagacttaga 1680 ttatctggca gcactggata atgatggaaa tctttctgaa tttggaatca tcatgtcaga 1740 gtttcctctt gatccacaac tctcgaagtc tatcttagcg tcctgtgaat ttgactgtgt 1800 agatgaagtg ctaacaatcg cagccatggt aacagctcca aattgctttt cacatgtgcc 1860 acatggagct gaagaggctg ccttgacttg ttggaagaca tttttacatc ccgaaggaga 1920 tcactttacc ctcatcagca tttacaaggc ttaccaagac acaactctga attctagcag 1980 tgagtactgt gtggaaaagt ggtgtcgtga ttacttcctc aactgttcag cactcagaat 2040 ggcagatgtt attcgagctg aactcttaga aattatcaag cgaatcgagc ttccctatgc 2100 agaacctgct tttggctcca aggaaaacac tctaaacata aagaaagctc ttctgtccgg 2160 ttactttatg cagattgctc gggatgttga tggatcaggt aactacttaa tgctgacaca 2220 taagcaggtt gctcagctgc atcccctgtc tggttactca atcaccaaga agatgccaga 2280 gtgggtcctc ttccataaat tcagcatttc tgagaacaac tacatcagga ttacctcaga 2340 aatctctcct gaactattta tgcagctggt accacaatac tatttcagta atctgcctcc 2400 tagtgaaagt aaggacattc tacagcaagt agtggatcac ctatcccctg tgtcaacaat 2460 gaataaggaa cagcaaatgt gtgagacgtg ccctgaaact gaacagagat gcactctcca 2520 gtgactcccc agcaaacaca aggtgcagca gggtcccaaa ggtagctgga tggctgaact 2580 gctggatatg ggagatacat gacgcgaaga cggatttcac atccacagga cggtcttgaa 2640 gaaaataaca ctgtgtatat tattttaaaa taaaaaatag aagtttttat tgagttcttt 2700 aaattactac tccatgcttt tcttcttctt ggaaaagttt ttaaatcaac cactcataat 2760 ttgaccaaaa ttttaaaaaa ctggtatttt gtaaatgtgt cagagacaca tgggacagaa 2820 ccctactttt tgtagaggaa cttaatctga ataaagtctg agtttttcag taaaaaaaaa 2880 aaaaaaaaaa aag 2893 70 885 DNA Homo sapiens misc_feature Incyte ID No 1454656CB1 70 ccagcatgcg gcgcccatgt aacccggtcc gtgccgcaaa gcgaacggcg gccgcggcgc 60 gggccccgcg ggggttagag gtcaccatgc tgagggtcgc gtggaggacg ctgagtttga 120 ttcggacccg ggcagttacc caggtcctag tacccgggct gccgggcggt gggagcgcca 180 agtttccttt caaccagtgg ggcctgcagc ctcgaagtct cctcctccag gccgcgcgcg 240 gatatgtcgt ccggaaacca gcccagtcta ggctggatga tgacccacct ccttctacgc 300 tgctcaaaga ctaccagaat gtccctggaa ttgagaaggt tgatgatgtc gtgaaaagac 360 tcttgtcttt ggaaatggcc aacaagaagg agatgctaaa aatcaagcaa gaacagttta 420 tgaagaagat tgttgcaaac ccagaggaca ccagatccct ggaggctcga attattgcct 480 tgtctgtcaa gatccgcagt tatgaagaac acttggagaa acatcgaaag gacaaagccc 540 acaaacgcta tctgctaatg agcattgacc agaggaaaaa gatgctcaaa aacctccgta 600 acaccaacta tgatgtcttt gagaagatat gctgggggct gggaattgag tacaccttcc 660 cccctctgta ttaccgaaga gcccaccgcc gattcgtgac caagaaggct ctgtgcattc 720 gggttttcca ggagactcaa aagctgaaga agcgaagaag agccttaaag gctgcagcag 780 cagcccaaaa acaagcaaag cggaggaacc cagacagccc tgccaaagcc ataccaaaga 840 cactcaaaga cagccaataa attctgttca atcatttaaa aaaaa 885 71 1269 DNA Homo sapiens misc_feature Incyte ID No 121130CB1 71 tcagacaagc actggacgtg gcggccattt tgttttggac accgagcagg agctggcggc 60 cgctgcagac gaaaggcagg aaagggcagg ccgggtgagc agacggatcg gccgactaga 120 cagccaacca gcaacaacga actgagctcg catactaccg cttacgcatc taaccaaccg 180 cccatctagc taacccgagc ccctccaccg tcaactcagg ttcggccggt ccccggcccg 240 cctgccggag ccgtggtggc agccccggga ggagcactgg cgtctgtttc cttcgattct 300 cgggattcga agatggctgc acagtcagcg ccgaaagttg tgctaaaaag caccaccaag 360 atgtctctaa atgagcgctt tactaatatg ctgaagaaca aacagccgac gccagtgaat 420 attcgggctt cgatgcagca acaacagcag ctagccagtg ccagaaacag aagactggcc 480 cagcagatgg agaatagacc ctctgtccag gcagcattaa aacttaagca gagcttaaag 540 cagcgcctgg gtaagagtaa catccaggca cggttaggcc gacccatagg ggccctggcc 600 aggggagcaa tcggaggacg aggcctaccc ataatccaga gaggcttgcc cagaggagga 660 ctacgtgggg gacgtgccac cagaacccta cttaggggcg ggatgtcact ccgaggtcaa 720 aacctgctcc gaggtggacg agccgtagct ccccgaatgg gcttaagaag aggtggtgtt 780 cgaggtcgtg gaggtcctgg gagagggggc ctagggcgtg gagctatggg tcgtggcgga 840 atcggtggta gaggtcgggg tatgataggt cggggaagag ggggctttgg aggccgaggc 900 cgaggccgtg gacgagggag aggtgccctt gctcgccctg tattgaccaa ggagcagctg 960 gacaaccaat tggatgcata tatgtcgaaa acaaaaggac acctggatgc tgagttggat 1020 gcctacatgg cgcagacaga tcccgaaacc aatgattgaa gcctgcccat cctcccatga 1080 gagactcttg ttagtcaaca catctgtaaa taaccttgag ataacagatg agaagaaatc 1140 tgattgatgc tggatggacc tatcacaata ggctgtggac ttacttgcca ccagcttgtg 1200 catttagtgt gttcctttta ctttttgata ctgtgttgta tgaaaccctt ttgtcctttg 1260 aaaaaaaaa 1269 72 1066 DNA Homo sapiens misc_feature Incyte ID No 1257715CB1 72 cggctcgagg tgaatggggg cagcatgagg ccgggcggct ttttgggcgc cggacagcgg 60 ctgagtagag ccatgagccg atgtgttttg gagcctcgcc ccccggggaa gcggtggatg 120 gtggctggcc tggggaatcc cggactgccc ggcacgcgac acagcgtggg catggcggtg 180 ctggggcagc tggcgcggcg gctgggtgtg gcggagagtt ggacgcgcga ccggcactgt 240 gccgccgacc tcgccctggc cccgctgggg gatgcccaac tggtcctgct ccggccacgg 300 cggcttatga acgccaacgg gcgcagcgtg gcccgggctg cggagctgtt tgggctgact 360 gccgaggaag tctacctggt gcatgatgag ctggacaagc ccctggggag actggctctg 420 aagctggggg gcagtgccag gggccacaat ggagtccgtt cctgcattag ctgcctcaac 480 tccaatgcaa tgccaaggct gcgggtgggt atcgggcgcc cggcgcaccc tgaggcggtt 540 caggcccatg tgctgggctg cttctcccct gctgagcagg agctgctgcc tctgttgctg 600 gatcgagcca ccgacctgat cttggaccac atccgtgagc gaagccaggg gccctcactg 660 gggccgtgac actagtggcc atggctgcct gcctgactgt agtgcccacc aacccagcca 720 ctgccacaga gctgccacgc cagccttggt atctactttt tatacaaatc tcctctagac 780 tgttccaggc tgcctgcgga ttaaagtggg ggtgactgtg actggaccag tccatttctg 840 gagtaggttc ttctctctgt gtcctacttg ggacgtaggg gaacttcagg aagactaaac 900 ttttcaagcc tttttagaga accaggggca cgcatctctc cttgggtggg ccatgggact 960 gtgactcctg gtggggacac gcagccttct gaggtctcgt ggccacagtg gagctgagca 1020 tgaccagcag ttgctgcagc atctccttgt gccatggctg gaacgt 1066 73 639 DNA Homo sapiens misc_feature Incyte ID No 1342022CB1 73 ggggagacac gtgcccttgg tactatgacc actagaccag cattcatatt acaccacagt 60 gactgcttct cgagccgctc gagccgaatt cggcacgagg gagtctggag acgacgtgca 120 gaaatggcac ctcgaaaggg gaaggaaaag aaggaagaac aggtcatcag cctcggacct 180 caggtggctg aaggagagaa tgtatttggt gtctgccata tctttgcatc cttcaatgac 240 acttttgtcc atgtcactga tctttctggc aaagaaacca tctgccgtgt gactggtggg 300 atgaaggtaa aggcagaccg agatgaatcc tcaccatatg ctgctatgtt ggctgcccag 360 gatgtggccc agaggtgcaa ggagctgggt atcaccgccc tacacatcaa actccgggcc 420 acaggaggaa ataggaccaa gacccctgga cctggggccc agtcggccct cagagccctt 480 gcccgctcgg gtatgaagat cgggcggatt gaggatgtca cccccatccc ctctgacagc 540 actcgcagga aggggggtcg ccgtggtcgc cgtctgtgaa caagattcct caaaatattt 600 tctgttaata aattgccttc atgtaaaaaa aaaaaaaaa 639 74 1420 DNA Homo sapiens misc_feature Incyte ID No 194704CB1 74 ggccgacgcg accatcgttt gtcgacgccg ctgccaccgc ctgcctgaga gaagtcgtcg 60 cggccgaccc cgtcgcctcc gccggctacc atgtccgccc aggcgcagat gcgggccctg 120 ctggaccagc tcatgggcac ggctcgggac ggagacgaaa ccagacagag ggtcaagttt 180 acagatgacc gtgtctgcaa gagtcacctt ctggactgct gcccccatga catcctggct 240 gggacgcgca tggatttagg agaatgtacc aaaatccacg acttggccct ccgagcagat 300 tatgagattg caagtaaaga aagagacctg ttttttgaat tagatgcaat ggatcacttg 360 gagtccttta ttgctgaatg tgatcggaga actgagctcg ccaagaagcg gctggcagaa 420 acacaggagg aaatcagtgc ggaagtttct gcaaaggcag aaaaagtaca tgagttaaat 480 gaagaaatag gaaaactcct tgctaaagcc gaacagctag gggctgaagg taatgtggat 540 gaatcccaga agattcttat ggaagtggaa aaagttcgtg cgaagaaaaa agaagctgag 600 gaagaataca gaaattccat gcctgcatcc agttttcagc agcaaaagct gcgtgtctgc 660 gaggtctgtt cagcctacct tggtctccat gacaatgacc gtcgcctggc agaccacttc 720 ggtggcaagt tacacttggg gttcattcag atccgagaga agcttgatca gttgaggaaa 780 actgtcgctg aaaagcagga gaagagaaat caggatcgct tgaggaggag agaggagagg 840 gaacgggagg agcgtctgag caggaggtcg ggatcaagaa ccagagatcg caggaggtca 900 cgctcccggg atcggcgtcg gaggcggtca agatctacct cccgagagcg acggaaattg 960 tcccggtccc ggtcccgaga tagacatcgg cgccaccgca gccgttcccg gagccacagc 1020 cggggacatc gtcgggcttc ccgggaccga agtgcgaaat acaagttctc cagagagcgg 1080 gcatccagag aggagtcctg ggagagcggg cggagcgagc gagggccccc ggactggagg 1140 cttgagagct ccaacgggaa gatggcttca cggaggtcag aagagaagga ggccggcgag 1200 atctgaaccc gtctcccggg tgctgtaaat agtctgataa acgttcacac agtctaaaat 1260 taccctttat atttgctgaa tacaactcat cttttgtagt ttaaaatttc tattgttttg 1320 gagctagctg tgagtttcta gaagtgtaca gagttgctcc tgtgttcccg ggtcatgttg 1380 agtaggaata aataaatctg atgctgccaa aaaaaaaaaa 1420 75 1457 DNA Homo sapiens misc_feature Incyte ID No 607270CB1 75 gcgccattag cgcctgcgcc gtctctaggc cccgccccct cacccctccg gtcctggagc 60 tcccacagct aacatggcgg cgccctgtgt gtcctacggc ggagcagttt cgtaccggct 120 tcttctctgg ggtaggggta gcctcgcccg gaagcaaggc ctctggaaaa ccgcggcccc 180 tgagttgcaa acaaatgtca gatcccagat attaaggcta agacatactg catttgtaat 240 accaaagaaa aacgttccta cctcaaaacg tgaaacttac acagaggatt ttattaaaaa 300 gcagattgaa gagttcaaca taggaaagag acatttagcc aacatgatgg gagaagatcc 360 agaaactttc actcaagaag atattgacag agctattgct taccttttcc caagtggttt 420 gtttgagaaa cgagccaggc cagtaatgaa gcatcctgaa cagatttttc caagacaaag 480 agcaatccag tggggagaag atggccgtcc atttcactat ctcttctata ctggcaaaca 540 gtcatactat tcattaatgc atgatgtata tggaatgtta ctcaatttag aaaaacatca 600 aagtcacttg caagccaaaa gtctgctccc agaaaaaact gtaaccagag acgtgattgg 660 cagcagatgg ctgattaagg aggaactaga agaaatgtta gtggaaaaac tgtcagatct 720 agattatatg cagttcattc ggctgctaga aaagttattg acatcgcagt gtggtgctgc 780 tgaggaagaa tttgtgcaga ggtttcgaag aagtgtaact cttgaatcaa aaaaacagct 840 gattgaacct gtacagtatg atgagcaagg aatggccttt agcaaaagcg aaggtaaaag 900 aaagactgca aaagcagaag caattgttta taaacatgga agtggaagaa taaaagtaaa 960 tggaattgat taccagcttt acttcccgat cacacaggac agagaacagc tgatgttccc 1020 tttccacttt gttgaccggc tgggaaagca cgacgtgacc tgcacagtct cagggggcgg 1080 gaggtcagcg caggctggag caatacgact ggcaatggca aaagccttgt gcagctttgt 1140 caccgaggac gaggtcgagt ggatgagaca agctggacta cttactactg atccacgtgt 1200 gagggaacgg aagaagccag gccaagaggg agcccgcaga aagtttacgt ggaagaaacg 1260 ctaagggttt gctcccagga aaggagagga agagctatat atatgtgccg acatgtggca 1320 gacacacagt aaataatggc tgaccagcat gagggcagta ctgtcagaaa tttctttgag 1380 ctgtgagatg gatttatttt taaatgctac tttgtaaagg tgacctttaa aaaataaaag 1440 gaaaataaag aaaaaaa 1457 76 1184 DNA Homo sapiens misc_feature Incyte ID No 758546CB1 76 caggccgtcc aggtcttggg gcgccgcggc ggaaatcgcg cggatgccag aacgcgctct 60 cagcttcggg tcctgcggct gcggctgccg ccatcatggt gcggaagctt aagttccacg 120 agcagaagct gctgaagcag gtggacttcc tgaactggga ggtcaccgac cacaacctgc 180 acgagctgcg cgtgctgcgg cgttaccggc tgcagcggcg ggaggactac acgcgctaca 240 accagctgag ccgtgccgtg cgtgagctgg cgcggcgcct gcgcgacctg cccgaacgcg 300 accagttccg cgtgcgcgct tcggccgcgc tgctggacaa gctgtatgct ctcggcttgg 360 tgcccacgcg cggttcgctg gagctctgcg acttcgtcac ggcctcgtcc ttctgccgcc 420 gccgcctccc caccgtgctc ctcaagctgc gcatggcgca gcaccttcag gctgccgtgg 480 cctttgtgga gcaagggcac gtacgcgtgg gccctgacgt ggttaccgac cccgccttcc 540 ttgtcacgcg cagcatggag gactttgtca cttgggtgga ctcgtccaag atcaagcggc 600 acgtgctaga gtacaatgag gagcgcgatg acttcgatct ggaagcctag cggatctccc 660 actttgcatg gctgtctttt acagatggga aaactgaggc ctgatgctgg agattctatg 720 agggtgctct cctcaagggt atcagacggt cgtaggttct taagaatttg attcatcagt 780 ggcaggccat gcatagagcc acgggaggtg cgtccttgtt ttccaggaaa tgttcttaga 840 acttggacta ctgattatta attgactgtg ccttgggaaa cagtgggaag taacttggtg 900 cagcactggg gtattgttgg cttcttgtgt tggaaacttt gtaatgtaaa aggaaaaact 960 ggaaatcccc acgccctgtt tccctttatc gtcttgtggt tggactggtt caattcgttt 1020 aactcgaatt cttgctcctg gccgtggtta agctgtgtac agatgatgga gagtttggcc 1080 tcaagttttt ataaactgag cgagactagt gttcaggatc tcctcccttg tttaaatgtc 1140 aataaatgcc ccaactgctt tgtaagtgca aaaaaaaaaa aaaa 1184 77 1638 DNA Homo sapiens misc_feature Incyte ID No 866043CB1 77 atcggggatc ttgccccagc cagaggctac agtggcccgg gaaggagcct caagtcacct 60 tccccatcaa agagccttct tgttcttctc tgtggacgag ccatgttcca gccagccaca 120 tgcccctggc agctgcccgc tttaagcaag taaaactctc caggaacttt cccaagtcat 180 ctttccgtgc tcaaagtgag tctgaaaccg tagtaaaaat ggcagctctt ttcagaagaa 240 aaaatgtgag gactgtgtgg taccctatac tcccagaaga ctaagacagc ggcaggcatt 300 aagcacggag acaggcaagg gtaaagacgt ggagccacag gggccccctg cagggcgtgc 360 cccagcccct ctctacgtgg gcccgggagt gtctgagttt attcagccgt atttgaatag 420 ccattataaa gaaaccacag ttccccggaa agtgcttttc cacctgagag gccacagggg 480 ccctgtcaac accattcagt ggtgtccagt cctttctaag agccacatgc ttctctccac 540 ttctatggat aaaactttca aggtatggaa cgccgtggac tccgggcact gcctgcagac 600 ctactccctg cacacagagg cagtgcgggc cgcccggtgg gctccctgtg gccggcgcat 660 cctcagtggt ggctttgact tcgcgctgca cctaacagac cttgaaacag gaacccagct 720 atttagtggt cgaagtgact ttagaatcac taccttgaaa ttccatccaa aagaccacaa 780 catcttttta tgtggaggct tcagctctga aatgaaagct tgggatataa ggactggcaa 840 ggtgatgaga agctacaagg cgaccatcca gcagaccttg gacatcctgt tcctccggga 900 aggctccgag ttcctgagca gcacagacgc ttccacccgg gactcagctg accgcaccat 960 tattgcctgg gatttccgga cctctgccaa aatctccaac cagattttcc acgagaggtt 1020 cacctgcccc agcctcgcct tgcacccgag agagcccgtg ttcctggcac agaccaatgg 1080 caactacctg gcccttttct ccactgtgtg gccctaccgg atgagcagac ggcggcgcta 1140 tgaagggcac aaggtggagg gctactcagt gggctgcgag tgctccccag gcggtgactt 1200 gctggtgacg ggcagcgccg atggccgggt cctgatgtac agcttccgca cagccagccg 1260 agcatgcaca ctgcaggggc acacacaggc ctgtgtcggc accacctatc accccgtgct 1320 gccctccgtc ctcgccacct gctcctgggg aggggacatg aagatctggc actgagcttt 1380 ttgtcactga accttcccga tgccagctgg gctcttggac tcccctcttc ctcaagggta 1440 gatgagagga acgagcacag aggttggctg tgggtcctgg gtaccacctt ctgagcctca 1500 gtttcctcat ctgtaaagtg gggagaaaag tctgtttgcc tcaggagtgt gaggactaca 1560 ctagtgaaag cgcctggcgg gcagccggcg atgcccaata aatgtgtgtt ttgctgtttg 1620 ttaagtgaaa aaaaaaaa 1638 78 701 DNA Homo sapiens misc_feature Incyte ID No 927065CB1 78 tcacgcttcg tggggcggga cgaggagaag ccaaacgtaa agacaccagg agtttctcgg 60 gcccagctgt ggctgctgcc ggggagcccc aagccttggc gggtccttgc ggcgaatagg 120 agtctggtca ggcgtcaggc tagtccgacg aagagtgggt gtgatcagca ctggaaaaga 180 tgcctgcccc tgctgccaca tatgaaagag tagtttacaa aaacccttcc gagtaccact 240 acatgaaagt ctgcctagaa tttcaagatt gtggagttgg actgaatgct gcacagttca 300 aacagctgct tatttcggct gtgaaggacc tgtttgggga ggttgatgcc gccttacctt 360 tggacatcct aacctatgaa gagaagacct tgtcagccat cttgagaata tgtagcagtg 420 gtcttgtcaa attgtggagc tctttgaccc tgttaaggat ccctattaaa ggcaaaaaat 480 gtgctttccg ggtgattcag gtttctccat ttcttcttgc attatctggt aatagtaggg 540 aactagtatt ggattgaatg aatagtcttc cattttggaa acgttcatcc actctcatat 600 ttattttttg gtgccctgca tgtttgaaga ctgaaagcag gctaaaagct cttgatgaaa 660 tttgagggtg ctgaaagatg ttcccactaa tttccagcca t 701 79 1829 DNA Homo sapiens misc_feature Incyte ID No 938071CB1 79 gggttttgca gaagtaccca gaactgtgtc caaggtttcc tcagatttgg gctgttccgc 60 agcggcaggt cccgggaacc aaggcaacag acatcttcct aggctcgcga gagcgccccc 120 ttgtcccacg gctgctgggg ccccccagta gccatggctc cggtgtccgg ctcacgcagc 180 ccggataggg aggcctcggg ctcgggggga agacgtcgca gttcgtcgaa gagtccgaag 240 cccagcaaat ctgcccgctc cccgcggggc cgccgctctc gctcgcactc ttgctctcgg 300 tccggggacc ggaatggact cacccatcag ctgggtggcc tcagccaagg ctcccgaaac 360 cagtcctacc gctcacgctc gcggtcgcgt tctagagagc ggccctctgc gccccggggc 420 atccccttcg cttctgcctc ctcgtcagtc tattacggca gctactcgcg cccctacggg 480 agcgacaagc cttggcctag cctcctcgac aaggagaggg aggagagcct gcggcagaag 540 agattaagtg agagagagag aattggagaa ttgggagctc ctgaagtatg gggactttct 600 ccaaagaatc ctgaaccaga ttctgatgaa catacaccag tggaggatga agagccaaag 660 aaaagcacta cttcagcttc tacttcagaa gaagaaaaaa agaagaagtc tagccgttca 720 aaagaaaggt ccaagaaaag gagaaagaaa aaatcatcga aaagaaaaca taagaagtat 780 tctgaagata gcgacagtga ctctgattct gaaacagact ccagtgatga agataacaaa 840 aggagagcaa agaaagccaa gaaaaaggaa aagaagaaga aacacagatc gaagaaatat 900 aagaaaaaga ggtctaagaa gagcagaaaa gagtccagtg attcaagctc taaagaatcc 960 caagaagagt ttctggaaaa tccctggaag gatcgaacaa aggctgaaga accatcagat 1020 ttaattggcc cagaggctcc aaaaacactt acctctcaag atgataaacc tttgaagcat 1080 cgccgaatgg aggctgtgcg actgcgaaaa gagaaccaga tctacagtgc tgatgagaag 1140 agagcccttg catcctttaa ccaagaagag agacgaaaga gagagaacaa gattctggcc 1200 agttttcgag aaatggttta cagaaagacc aaagggaagg atgacaaata aagattttct 1260 gattgtccag aagacatttt taacaacaaa aaagaaagtc tgggttccac acatacatag 1320 aaaaagatta ttatgttctg agaaagcttt acagtgctac tgtgccttct atttaattct 1380 ttcagtcctt caataaaaag ctgcttattg atataacttt agcaagttct ttgggttatt 1440 ttggattgac catagtaact ttctggttta aaaatccaaa ttatgggctg ggcacggttg 1500 ctcacgcctg tagtctcagc ctcctgaaat gctgggattg caggtgtgag caaccgtgcc 1560 tggccgtttt tgttaaggtt atttgatctg cattattatt acatgcctat gataaatttt 1620 taattacccc tgtgtataaa agggctttcc gattatccta ttgggaaaat gcccgcttgc 1680 cttatatttt taagtggttg tttttcaaaa gtgtttaaat aagggcggcc atatttcaaa 1740 gtattggaca aaaagttttt ttaattataa tttttggaga cgggggtctc ctctgttacc 1800 caggctagag ttcagttgac cgagatctt 1829 80 2541 DNA Homo sapiens misc_feature Incyte ID No 3295984CB1 80 caagaaagag gggaaaggat cggaaaaaga agctaaaata ctatagaaaa ccatgagatc 60 tattcgatct tttgctaatg atgatcgcca tgttatggtg aaacattcaa caatctatcc 120 atctccggag gaacttgaag ctgttcagaa tatggtatct actgttgaat gtgctcttaa 180 acatgtctca gattggttgg atgaaacaaa taaaggcaca aaaacagagg gtgagacaga 240 agtgaagaaa gatgaggccg gagaaaacta ttccaaggat caaggtggtc ggacattgtg 300 tggtgtaatg aggattggcc tggttgcaaa aggcttgctg attaaagatg atatggactt 360 ggagctggtt ttaatgtgca aagacaaacc cacagagacc ctgttaaata cagtcaaaga 420 taatcttcct attcagattc agaaactcac agaagagaaa tatcaagtgg aacaatgtgt 480 aaatgaggca tctattataa ttcggaatac aaaagagccc acgctaactt tgaaggtgat 540 acttacctca cctctaatta gggacgaatt ggagaagaag gatggagaaa atgtttcgat 600 gaaagatcct ccggacttat tggacaggca gaaatgcctg aacgccttgg cgtctcttcg 660 acatgccaaa tggtttcagg caagggcaaa tggattaaaa tcatgtgtaa ttgtcctccg 720 cattctgcgt gatttgtgca acagagtccc cacatgggca ccattgaaag gatggccact 780 agaacttata tgtgaaaagt ctataggtac ttgtaataga cctttgggcg ctggggaggc 840 cttgagacga gtaatggagt gtttggcatc tggaatacta cttcctgggg gtcctggtct 900 tcatgatcct tgtgagcgag acccaacaga tgctctgagc tatatgacca tccagcaaaa 960 agaagatatt acccacagtg cacagcatgc actcagacta tcagcctttg gtcagattta 1020 caaagtgctg gagatggacc cccttccatc tagtaagcct tttcagaagt attcctggtc 1080 agttactgat aaagaaggtg ctgggtcttc agctctaaag aggccatttg aagatggatt 1140 aggggatgat aaagacccca acaagaagat gaaacgaaac ttaaggaaaa ttctggatag 1200 taaagcaata gaccttatga atgcactaat gaggctaaat cagatcaggc ctgggcttca 1260 gtataagctc ctatctcagt ctggccccgt tcatgcccca gtcttcacaa tgtctgtaga 1320 tgtggatggc acaacatatg aagcctcagg accatccaag aaaacagcaa aacttcacgt 1380 agcggtgaag gtattgcagg caatgggata tccaacaggc tttgatgcag atattgaatg 1440 tatgagttcc gatgaaaaat cagataatga aagtaaaaat gaaacagtgt cttcaaactc 1500 aagcaataat actggaaatt ctacaactga aacctccagt accttagagg taagaactca 1560 gggccctatc ctcacagcaa gtggcaaaaa ccctgtaatg gagctcaatg aaaaaagaag 1620 aggtctcaag tatgaactca tctcagagac tggtggaagc catgacaagc gctttgtaat 1680 ggaggtagaa gtagatggac agaaattcag aggcgcaggt ccaaataaga aagtggcaaa 1740 ggcgagtgca gctttagctg ccttggagaa actgttttct ggacccaatg cggcaaataa 1800 taagaaaaag aagattatcc ctcaggcaaa gggcgttgtg aatacagctg tgtctgcagc 1860 agtccaagct gttcggggca gaggaagagg aactctaaca aggggagctt ttgttggggc 1920 gacagctgct cctggctaca tagctccagg ctatggaaca ccatatggtt acagcacagc 1980 tgcccctgcc tatggtttac ccaagagaat ggttctgtta cccgttatga aatttccaac 2040 atatcctgtt ccccactact cattctttta gcaaatgaca gaagctaatt cctattgaac 2100 aacaatacag tacaacacag aatgttagag aaaaagcctt tttatcctgc tttctttgaa 2160 cacatacttg atcaaaatta tttgtaaaga acatctttcc tactttttga ttttaacaaa 2220 tgcaaattta gttctctaaa acttgaaaaa aaaaaaagaa accagttctg tgaaaacggt 2280 acctcatttc tggaaaataa cttataccag cccttctgtt ctagggaaat aaaagtctag 2340 cagttcaaag tttaagtttt aagagacgta tcagattatg taaaattaaa tttgtgaagg 2400 atgtatagag tctcaaacac tgatcacaaa taaactgctt tgttgtaaca cagagtactg 2460 cctggttcct gatgcagtca ctgattctta gttgattgat atgtatttgc cccagggcac 2520 tttaatttgg gctgtagtta t 2541 81 1647 DNA Homo sapiens misc_feature Incyte ID No 4545237CB1 81 gtccgcggtc ggccgggctc cgcctgcagt gtggcccgtc cggacagtcc ctcaccccgg 60 cctgcgctgc tgcgtggact cgggcctcag gaattccgct gcggcccaag gcttgccgtt 120 tgacgaggag cagtcgcggt aggcggtggg caaggctgcc ctgggcggag gccgaggcgc 180 ggctcggact ccagcatggc gaccgcggtg cgcgctgtgg gctgcctccc cgtgctgtgt 240 agcgggacgg caggtcattt attggggagg cagtgttccc taaacacctt accagcagct 300 tccattttgg catggaagag tgttctcggc aatggccatt tgtcatcact gggaaccaga 360 gacacccatc cctacgccag cttgagccgt gcactgcaga cacaatgctg tatttcttct 420 cccagtcacc tgatgagcca gcagtataga ccatatagtt tcttcactaa attgactgca 480 gatgagctgt ggaaaggcgc tttagcagag actggtgctg gagcaaaaaa aggaagaggc 540 aaaagaacta aaaagaagaa aagaaaggat ctgaacaggg gtcagatcat tggtgaaggg 600 cgttatggtt ttctatggcc cggactgaat gtccctctta tgaaaaatgg agcagtgcag 660 accattgccc aaagaagcaa ggaagagcag gagaaggtgg aggcagacat gatccagcag 720 agagaagagt gggaccgaaa gaagaagatg aaggttaaac gggagcgagg atggagtgga 780 aactcatggg gaggcatcag tcttggcccc cctgaccctg gtccctgtgg agaaacatat 840 gaggattttg ataccaggat acttgaggta agaaacgttt tcactatgac tgcgaaagag 900 ggaagaaaga aatcgatccg tgtcttggtg gctgtgggga acggaaaagg agctgcaggt 960 ttttctattg ggaaagctac tgatcggatg gatgctttca ggaaagcaaa gaacagagca 1020 gttcaccatt tgcattatat agaacgatat gaagaccata caatattcca tgatatttca 1080 ttaagattta aaaggacgca tatcaagatg aagaaacaac ccaaaggtta cggcctccgc 1140 tgccacaggg ccatcatcac catctgccgg ctcattggca tcaaagacat gtatgccaag 1200 gtctctgggt ccattaatat gctcagcctc acccagggcc tcttccgtgg gctctccaga 1260 caggaaaccc atcaacagct ggctgataag aagggcctcc atgttgtgga aatccgggag 1320 gaatgtggcc ctctgcccat tgtggttgcg tccccccggg ggcccttgag gaaggatcca 1380 gagccagaag atgaggttcc agacgtcaaa ctggactggg aagatgtgaa gactgcacag 1440 ggaatgaagc gctctgtgtg gtctaatttg aagagagccg ccacgtaacc tctctggcct 1500 tgtgcagcca gttcctgtgc tgccctgcac ctaggagaga ctcagcccct cacagcttgg 1560 gatgttacct tgccttttgt ttgttttgag ggaagtttaa tctttaaact ctttggaaat 1620 aaataattat agctttcaaa aaaaaaa 1647 82 735 DNA Homo sapiens misc_feature Incyte ID No 4942964CB1 82 ctcgttcctg tcgcgcagca cgacctccac ttccacatct cccccggcgt cggcgcggtc 60 agttgaacca tggcggactc caaggccacc tcggcggtca ccctccgcac ccgcaagttc 120 atgaccaacc gcctcctggc ccgcaagcaa ttcgtgcttg aggtgatcca ccccggccgc 180 gccaacgtct ccaaggcgga gttgaaggag aggcttgcca aggcgtacga ggtgaaggac 240 cccaacacca tctttgtctt caagttccgc acccacttcg gaggaggaaa gtccactggt 300 ttcggcctca tctacgacaa cctcgaggct gccaagaagt tcgagccgaa ataccgcctc 360 atcaggaatg gtcttgctac taaggttgag aagtcccgca agcaaatgaa ggagcggaag 420 aacagggcca agaagatccg tggtgtcaag aagaccaaag ctggtgacgc caagaagaag 480 taaacgttcg tttacatttg tattactgtt ctgggctctg ggtggtctag ctgcaatgtc 540 ataattatgg tcgtgttagg ttttgttcca cccttggcac tgaagtgatt ttttttgtaa 600 ttcctcggca ctgaagtgaa gttttgtctg aatattgcct cgtaacataa ttgcccggtc 660 cctgttctag ttgtggcgca gtctggtttg ttttgacatt tgtaatcgtg gttaatgtgg 720 ntggatcggt tcatg 735 83 2614 DNA Homo sapiens misc_feature Incyte ID No 5702144CB1 83 gtgcgctctc acccttatct ccaaattctg ggtgttgtcg cgagggctgc tgtgtccgga 60 acttccggtt ccggtcaggg tccgcgatct cggactaagg atgcggtccc gggttctgtg 120 gggcgctgcc cggtggctct ggccccgccg ggccgttggc ccagcccgcc ggcccctgag 180 ctccggtagc ccgccgctgg aggagctgtt cacccggggc gggcccttgc ggaccttcct 240 cgagcgccag gcggggtctg aagcccattt gaaggtcagg aggcccgagt tgctggcggt 300 gatcaaactg ctgaacgaga aggagcagga gctgcgggag actgagcact tgctgcacga 360 tgagaatgaa gatttaagga aacttgcaga gaatgaaatc actttgtgtc aaaaagaaat 420 aactcagctg aagcatcaga ttatcttact tttggttccc tcagaagaaa cagatgaaaa 480 tgatttgatc ctggaagtaa ctgcaggagt tggaggtcag gaggcaatgt tgtttacatc 540 agagatattt gatatgtatc agcaatatgc tgcatttaaa agatggcatt ttgaaaccct 600 ggaatatttt ccaagtgaac taggtggcct tagacatgca tctgccagca ttgggggttc 660 agaagcctat aggcacatga aatttgaagg aggtgttcac agagtacaaa gagtgccaaa 720 gacagaaaag caaggccgca tccatactag caccatgact gtagcaatat taccccagcc 780 tactgagatt aatctggtga ttaatccgaa agatttgaga attgacacta agcgagccag 840 tggagctggg gggcagcatg taaataccac ggacagtgct gtccggatag ttcatcttcc 900 aacaggtgtt gtttctgaat gtcaacaaga gagatctcag ctgaaaaata aagagctggc 960 tatgacaaag ttacgtgcaa aactgtacag catgcatcta gaagaagaaa taaataaaag 1020 acagaatgct agaaaaattc agattggaag taaaggaaga tcagagaaaa taagaacata 1080 taattttcca cagaaccggg tcacagatca cagaataaac aagacgctgc atgatcttga 1140 aacttttatg caaggagatt atctactgga tgaacttgta cagtcattga aggaatacgc 1200 cgattatgaa tctttagtag aaattatttc ccaaaaagtt taagttgatt tgttatttat 1260 agactttcgt agcttagaaa aattctacag tacatccaca tagggtgaaa gtacccttac 1320 tctcttgaaa aacgttgagt taacacagtt ggaggtaata tgcatattct gaagtcatag 1380 ataatttaca cagatctctc tcaatgcatt agcaaaaatc atacaatata cagatggtcc 1440 tcgatttaca ttgtggttaa ttcccaataa acccatcata agttaaaaat gcatataacg 1500 ttagcaacac agcagtctcc taattaatga cagcttgact taacaatttt ccaactttac 1560 catggtgtga aagaggtatg attcctaagc cctaaggagc tcctcagctt gaaatggggc 1620 tgcatcccta taaacccatc ataaagtcaa aaaatcctaa aacataagtt ggtgaccatc 1680 tgtaatcatg atgtggtggt aaatcttgga cgctacctta caataactag acaaaggaaa 1740 atcatccttt gtcctgttct gtgtaaatat ttaatgaatg atcaaaactt cagtttaaat 1800 attatgaaaa actttaaaca taaagtagta gaaataagac agtaaatact gtatcctaat 1860 atccagtcag gatacagaaa ccataccatt aacttgaaca gggataattt taatataaaa 1920 actgttaact gataatggta ttaactttta agagggatga aagagagcta tgatgtccta 1980 ggactgagag taccccagga aagaataccc ttgaaagggt ctccccttcc ccatggtgaa 2040 gtcaggccta atggagagag tggctacagc ctactcagtg attgggaaat tccctgtctt 2100 gccctgggcc agagctggtg taccgctggt ggatcaggtc ttacaagcaa agaacctcac 2160 actcccaact ggtaagccag aagcctcttg ctagggtgtg agcaaaactt ggacaggaac 2220 tctcagtaga tgtttgtgtt tgtcaagatt ctccagacaa acttccttaa aaggattggc 2280 ttgtgttgtt attattaagt ctaacaagtc caaaagctgg agtgtgaggc aggaggctgg 2340 aaacccagga aagctgatgg tgcaaggtcc agtccaaagg tatctgttgg aggattctct 2400 tgttctggga agaggacggt ctttttttct cttcagacct tcacctgact ggatcaagcc 2460 cactaacatc gaggaggaca gtctgcatta ctcagagttc actgattgat ttaaatgtca 2520 atctcatata aaacaccctc acagaaacac ctagaataat gtttgacctt ataattggaa 2580 aatcagagca aaagttaaat ctctaaaaaa aaaa 2614 84 736 DNA Homo sapiens misc_feature Incyte ID No 5862945CB1 84 actcggcggc ttccgtagcg ggagggcgaa agatggcggc ggcagtactg ggacagttgg 60 gtgcgttatg gatacataac ctgaggagcc gggggaagct ggccttgggt gttttacctc 120 aatcatatat ccacacaagt gcttctcttg acatttctcg aaaatgggag aagaagaata 180 aaattgttta tcctccacaa ctgcctggag aacctcggag accagcagaa atctaccact 240 gtcgaagaca aataaaatat agcaaagaca agatgtggta tttggcaaaa ttgatacgag 300 gaatgtctat tgaccaggct ttggctcagt tggaattcaa tgacaaaaaa ggggccaaaa 360 taattaaaga ggttctctta gaagcacaag atatggcagt gagagaccat aacgtggaat 420 tcaggtccaa tttatatata gctgagtcca cctcaggacg aggccagtgc ctgaaacgca 480 tccgctacca tggcagaggt cgctttggga tcatggagaa ggtttattgc cattattttg 540 tgaagttggt ggaagggccc ccacctccac ctgagccacc aaagacggca gttgcccatg 600 ccaaagagta tattcagcag cttcgcagcc ggaccatcgt tcacactcta tgatgaggag 660 attcagactc cacagtgtat atattttgcc atttattttc taaaaataaa caaaaattga 720 aggcaaaaaa aaaaaa 736 85 1046 DNA Homo sapiens misc_feature Incyte ID No 6319547CB1 85 ggcgtaacgc gtcacgggcg gcctggcagc tggcggcatt gaggcggacg cgtctagagg 60 tccgtctgac cgcggcgtcg ggacctggtt tccgggcatg agctgagagc accacgccga 120 ggccacgagt atttcataga cattgatgga agcagaaacc aaaactcttc ccctggagaa 180 tgcatccatc ctttcagagg gctctctgca ggaaggacac cgattatgga ttggcaacct 240 ggaccccaaa attaccgaat accacctcct caagctcctc cagaagtttg gcaaggtaaa 300 gcagtttgac ttcctcttcc acaagtcagg tgctttggag ggacagcctc gaggctactg 360 ttttgttaac tttgaaacta agcaggaagc agagcaagcc atccagtgtc tcaatggcaa 420 gttggccctg tccaagaagc tggtggtgcg atgggcacat gctcaagtaa agagatatga 480 tcataacaag aatgataaga ttcttccaat cagtctcgag ccatcctcaa gcactgagcc 540 tactcagtct aacctaagtg tcactgcaaa gataaaagcc attgaagcaa aactgaaaat 600 gatggcggaa aatcctgatg cagagtatcc agcagcgcct gtttattcct actttaagcc 660 accagataaa aaaaggacta ctccatattc tagaacagca tggaaatctc gaagatgatg 720 gttgtgaatt actgtagcag caaaagcaaa ttggtctcca cacctaaaat cgtctgcctg 780 tgtactttgt agatgtgaat ggtactattc aacggagcac aatcacatgt tagcatttgg 840 taacataatg tttttggatg ttcttatgga tgtttcttcc ctaaactatg tatggaattg 900 agcatcatcc agaataaata gcgttgtatc ccaaattgtg atttgaaccc tgggatgctc 960 taattggctg gttggtttgg atttgtaact ccagaaacat tctatagtgt gccagagcaa 1020 aaggcaaata cacaaaatat tatttt 1046 86 2266 DNA Homo sapiens misc_feature Incyte ID No 000124CB1 86 cgcgttcacc agcccggaag tgcgcgtggc ggcggtggcg gctgcggcaa cagcggggcc 60 gatgtgtagt tggtgactgc ctctccagat gctgaggtgc ctgtatcatt ggcacaggcc 120 agtgctgaac cgtaggtgga gtaggctgtg ccttctgaag cagtatctat tcacaatgaa 180 gttgcagtct cccgaattcc agtcactttt cacagaagga ctgaagagtc tgacagaatt 240 atttgtcaaa gagaatcacg aattaagaat agcaggagga gcagtgaggg atttattaaa 300 tggagtaaag cctcaggata tagattttgc caccactgct acccctactc aaatgaagga 360 gatgtttcag tcggctggga ttcggatgat aaacaacaga ggagaaaagc acggaacaat 420 tactgccagg cttcatgaag aaaattttga gattactaca ctacggattg atgtcaccac 480 tgatggaaga catgctgagg tagaatttac aactgactgg cagaaagatg cggaacgcag 540 agatctcact ataaattcta tgtttttagg ttttgatggc actttatttg actactttaa 600 tggttatgaa gatttaaaaa ataagaaagt tagatttgtt ggacatgcta aacagagaat 660 acaagaggat tatcttagaa ttttaagata cttcaggttt tatgggagaa ttgtagacaa 720 acctggtgac catgatcctg agactttgga agcaattgca gaaaatgcaa aaggcttggc 780 tggaatatca ggagaaagga tttgggtgga actgaaaaaa attcttgttg gtaaccatgt 840 aaatcatttg attcacctta tctatgatct tgatgtggct ccttatatag gtttacctgc 900 taatgcaagt ttagaagaat ttgacaaagt cagtaaaaat gttgatggtt tttcaccaaa 960 gccagtgact cttttggcct cattattcaa agtacaagat gatgtcacaa aattggattt 1020 gaggttgaag atcgcgaaag aggagaaaaa ccttggctta tttatagtta aaaataggaa 1080 agatttaatt aaagcaacag atagttcaga cccattgaaa ccctatcaag acttcattat 1140 agattctagg gaacctgatg caactactcg tgtatgtgaa ctactgaagt accaaggaga 1200 gcactgtctc ctaaaggaaa tgcagcagtg gtccattcct ccatttcctg taagtggcca 1260 tgacatcaga aaagtgggca tttcttcagg aaaagaaatt ggggctctat tacaacagtt 1320 gcgagaacag tggaaaaaaa gtggttacca aatggaaaaa gatgaacttc tgagttacat 1380 aaagaagacc taaaactgat ggctactaaa aagcagagca tttctggtaa gactaaattt 1440 tctcccctcc ctcttaatga ggttttagag actacaccag aataaaagac agtttagggg 1500 acctctgtag aacaacaagg gtcttatttt gtgaattata tatttcaaga actaaacaga 1560 gatccacctt tctggatctg atttatatca ctgaaatgta cagttctttt ggaatagttt 1620 cacctgagaa aacatagttg gctattatct atcttaacct gttcaggctt ttaaaaaaaa 1680 ctgtttttgc atagggtagt actaagatct taaaaagtgg taactgtctt gaagaaaaaa 1740 cgtttattgt ttgtttgcaa ttgaaataac agggttacct taacaatgac tgtctatgat 1800 gtgtcagttc ttatctgaat tccaaaataa acctgtgctt aaaaaagaaa taattgacca 1860 agtaagtttg cataaaatgt gaatactaaa tgtgtcccca gttgctggca ttcatatgta 1920 caggatttgt tctagcaagc tatgcttcag tatgtggttg atatttttct gtcacaatga 1980 tttctttatg catgcagagc ctgggaaagt catgggatta acttgagggt cactattgag 2040 cctattaatt aattaattat tgttttaata aaacaaacat tggtattgga agataaatat 2100 gtttatgtgg tatctgacaa tgtgtattag gtgtcatata caatggtaat atgcctgtct 2160 ttaaagtgtt attttattaa ttaaaaggat atggctatta ttatatattc tctaaagatt 2220 tattctctaa agatttgagt cctaaatgct ttcatcacgg cacgag 2266 87 1041 DNA Homo sapiens misc_feature Incyte ID No 1659474CB1 87 caagcagcat ggctgcaggt tgctcagagg cgccgcggcc aacggcggct tctgatgggt 60 ctctggtagg gcaggctggc gtcctgcctt gcctagagtt gccgacttat gccgctgctt 120 gtgcgctggt gaacagtcgc tactcatgcc tggtggccgg gccgcaccaa aggcacatcg 180 cgctgtcgcc ccgctacctt aacaggaaac gcaccggcat tcgagaacag cttgatgcgg 240 agctccttcg ctattctgag agccttttag gtgtccctat tgcatatgat aacatcaaag 300 ttgtgggaga gcttggagat atttatgatg atcaaggaca cattcatctt aacattgaag 360 ccgattttgt tattttctgc cctgaaccgg ggcagaagct tatgggtata gttaataaag 420 tgtcttctag ccacattggc tgtttagtac atgggtgttt caatgcctcc attcctaaac 480 ctgagcagtt gtcagctgag cagtggcaaa ccatggagat aaacatgggt gatgaactag 540 aatttgaagt atttcgttta gactcagatg ctgctggagt attctgcatt cggggaaaac 600 taaatatcac aagtttacaa ttcaagcgct ctgaagtttc tgaagaagtt acagaaaatg 660 gcactgagga agctgctaaa aaacctaaaa agaagaaaaa gaagaaagac ccagagacat 720 atgaagtgga cagtggtacc acaaagctag cagatgatgc agatgacact ccaatggaag 780 agtcagccct gcagaatact aataatgcga atggcatctg ggaggaggag ccaaagaaaa 840 agaagaagaa gaaaaagcac caggaagttc aggaccagga ccctgttttc caaggcagtg 900 actccagtgg ttaccaaagt gaccataaaa agaaaaaaaa agaaaagaaa accaacagtg 960 aagaggccga atttacccca cctttgaaat gctcaccaaa aagaaaaggg aaaagtaatt 1020 ttctttagtg tattttaaac a 1041 88 2722 DNA Homo sapiens misc_feature Incyte ID No 2267892CB1 88 cgctttctgg gtaaagatgg acgtccacga tctctttcgc cggctcggcg cgggggccaa 60 attcgacacg agacgcttct cggcagacgc agctcgattc cagataggaa aaaggaaata 120 tgactttgat tcttcggagg tgcttcaggg actggacttt tttggaaaca agaagtctgt 180 cccaggtgtg tgtggagcat cacaaacaca tcagaagccc caaaatggag agaaaaaaga 240 agagagccta actgaaagga agagggagca gagcaagaaa aaaaggaaga cgatgacttc 300 agaaattgct tcccaagaag aaggtgctac tatacagtgg atgtcatctg tagaagcaaa 360 gattgaagac aaaaaagttc agagagaaag taaactaact tccggaaagt tggagaatct 420 cagaaaagaa aagataaact tcttgcggaa taaacacaaa attcacgtcc aaggaaccga 480 tcttcctgac ccaattgcta catttcagca acttgaccag gaatataaaa tcaattctcg 540 actacttcag aacattctag atgcaggttt ccaaatgcct acgccaatcc aaatgcaagc 600 catcccagtt atgctgcatg gtcgggaact tctggcttct gctccaactg gatctggaaa 660 aacattagct tttagcattc ctattttaat gcagctgaaa caacccgcaa ataaaggctt 720 cagagccctg attatatcac caacacgaga acttgccagc cagattcaca gagagttaat 780 aaaaatttct gagggaacag gattcagaat acacatgatc cacaaagcag cagtggcagc 840 caagaaattt ggacctaaat catctaaaaa gtttgatatt cttgtgacta ctccaaatcg 900 actaatctat ttattaaagc aagatccccc cggaatcgac ctagcaagtg ttgagtggct 960 tgtagtagac gaatcagata aactgtttga agatggcaaa actgggttca gagaccagct 1020 ggcttccatt ttcctggcct gcacatccca caaggtccga agagctatgt tcagtgcaac 1080 ttttgcatat gatgttgaac agtggtgcaa actcaacctg gacaatgtca tcagtgtgtc 1140 cattggagca aggaattctg cagtagaaac tgtagaacaa gagcttctct ttgttggatc 1200 tgagaccgga aaacttctgg ccatgagaga acttgttaaa aagggtttca atccacctgt 1260 tcttgttttt gttcagtcca ttgaaagggc taaagaactt tttcatgagc tcatatatga 1320 aggtattaat gtggatgtta ttcatgcaga gagaacacaa caacagagag ataacacagt 1380 ccacagtttc agagcaggaa aaatctgggt tctgatttgt acagccttgc tagcaagagg 1440 gattgatttt aaaggtgtga acttggtgat caactatgac tttccaacta gctcagtgga 1500 atatatccac aggataggtc gaactggaag agcagggaat aagggaaaag caattacatt 1560 tttcactgag gatgataagc cattattaag aagcgttgct aatgttatac agcaggctgg 1620 gtgtcctgta ccagaataca taaaaggttt tcagaaacta ctaagcaaac aaaagaaaaa 1680 gatgattaag aaaccattgg aaagggagag cattagtaca actccaaaat gtttcttaga 1740 aaaagctaag gataaacaga aaaaggtcac tggtcagaac agcaagaaga aagtagctct 1800 tgaagacaaa agttaaaaac agactttaaa aatactgtcc cagaaatgta attttatgat 1860 cccagcatga atgttatttt catggaatac ttgaagtctt acagtcacct gtaccaaaca 1920 tttgaaatca actacaagta catgggactg gtgataaatg atcctaaact atcaagtcag 1980 tttcaatttg taggtgcctt ttttttttcc tgtagagatg agggtcttgc catgttgtcc 2040 aggctggtct tgaactcctg acctcacaca atcctcctgc cttagcctcc tgagtaactg 2100 agattacagg cacaagctgc tgcacccagc tctgtaggtg acttttaaat gattatacaa 2160 tggaaataac attcattgac atttctgtgg tttgaatcca gagagatact tcttatagaa 2220 aaacaaatgt ttatgctaaa aataacacca aaatgtggtg aactcttaag gacttttccc 2280 ttcaagtgtg aaggaaggtg tgatgaatgc tgtggagagg catctggaac agaaattcaa 2340 aataaagcct tgacattaaa taccccttcc actgctcact ttgtggatgg tagcatgagc 2400 tgtctaccaa gaagaaacct gctgctctct taattttaat atttcctaat ttgttgatgg 2460 ccttttgtgt tgtgaaccac aacaaagaga ggcctctttt gtggctggtt attccagttc 2520 cctgggattt taaattcttt ggtctattaa gtatccttgt attggatacg taatacctta 2580 gtgctgtcat aatgttgtac aagatcatga tcagcttctc cctttcttca ttttctgtga 2640 tttaaccatg ttctttcctg tctctttcca tttaagatat tttatttgaa tactgataaa 2700 cattttatcc cccccctttg gg 2722 89 1287 DNA Homo sapiens misc_feature Incyte ID No 2670307CB1 89 ccaagagtct aggtaagagt ttgttcccgt ggtgcggagg gtcaaggccc acacccggaa 60 acctagcgag gtaaagttgc gtcttggttg tagagacgac aacttctccg cttcctcggc 120 gatggcggcg tccgggagcg gtatggccca gaaaacctgg gaactggcca acaacatgca 180 ggaagctcag agtatcgatg aaatctacaa atacgacaag aaacagcagc aagaaatcct 240 ggcggcgaag cctggactaa ggattcacca ttactttaag tactgcaaaa tctcagcatt 300 ggctctgctg aagatggtga tgcatgccag atcgggaggc aacttggaag tgatgggtct 360 gatgctagga aaggtggatg gtgaaaccat gatcattatg gacagttttg ctttgcctgt 420 ggagggcact gaaacccgag taaatgctca ggctgctgca tatgaataca tggctgcata 480 catagaaaat gcaaaacagg ttggccgcct tgaaaatgca atcgggtggt atcatagcca 540 ccctggctat ggctgctggc tttctgggat tgatgttagt actcagatgc tcaatcagca 600 gttccaggaa ccatttgtag cagtggtgat tgatccaaca agaacaatat ccgcagggaa 660 agtgaatctt ggcgccttta ggacataccc aaagggctac aaacctcctg atgaaggacc 720 ttctgagtac cagactattc cacttaataa aatagaagat tttggtgtac actgcaaaca 780 atattatgcc ttagaagtct catatttcaa atcctctttg gatcgcaaat tgcttgagct 840 gttgtggaat aaatactggg tgaatacgtt gagttcttct agcttgctta ctaatgcaga 900 ctataccact ggtcaggtct ttgatttgtc tgaaaagtta gagcagtcag aagcccagct 960 gggacgaggg agtttcatgt tgggtttaga aacgcatgac cgaaaatcag aagacaaact 1020 tgccaaagct acaagagaca gctgtaaaac taccatagaa gctatccatg gattgatgtc 1080 tcaggttatt aaggataaac tgtttaatca aattaacatc tcttaaacag tctctgagaa 1140 gtactttacc tgaaagacag tatgagaaaa atattcaagt aacactttaa aaccagttac 1200 ccaaaatctg attagaagta taaggtgctc tgaagtgtcc taaatattaa tatcctgtaa 1260 taaagctctt taaaatgaaa aaaaaaa 1287 90 2226 DNA Homo sapiens misc_feature Incyte ID No 4524210CB1 90 cggctcgagc cggaagcgac tttccgccga gaaatagggg gcgcgtgttt ggaaattgat 60 agaaaagata aagggaccga gctgctgtca gcctggctta ctgatctgcg tccgtttcac 120 cacggattca gttactaagc atttttttct ttttttggtt ctttgcaacg tgagtggcat 180 tggctcagtg atttccatga gcatctctac cagaaaacat tgcctcgatg aggtgtggtg 240 gaagcccggc agccccttct aatcggctag gcttgagaaa gcgtgtacct ctgcatttcc 300 gaaattaact cagcgtgatc ggcaagattt tcctcagcat ctggtgtcaa gacactcgtc 360 actattaatt cggaaagaaa aaaaaaaaca aaacaccgtt ttccagcatt tctctttgtg 420 gagaactaaa caacaggaaa aatgtctatt ttccctaaga tatctttgag acctgaggtt 480 gaaaactatc ttaaggaagg ctttatgaat aaggagattg tgactgcttt aggtaaacaa 540 gaagcagaaa ggaagtttga aactttgtta aagcacctgt cacatcctcc atcatttaca 600 actgtcagag tgaatacaca tttagcctca gtacaacatg tgaaaaatct gttacttgat 660 gaacttcaga agcagtttaa tggattaagt gttcctattc ttcaacatcc agaccttcaa 720 gatgtgttac ttattcctgt tattggaccc agaaagaata ttaaaaaaca acagtgtgaa 780 gccattgttg gagcccagtg tggcaatgca gttttaagag gagcccatgt ctatgcccca 840 ggaattgtgt cagcatcaca atttatgaaa gctggagatg ttatttctgt atactctgat 900 attaaaggaa aatgtaagaa aggagccaaa gaatttgatg gaacaaaagt atttcttgga 960 aatgggattt ctgaactaag ccgcaaagaa atcttcagtg gattacctga actgaaaggc 1020 atgggcataa gaatgacaga accagtatat ctcagccctt catttgacag tgtactgccc 1080 cgttacttat ttttacaaaa tttgccatct gccttagtaa gtcatgtact aaatcctcaa 1140 cctggagaga agattctaga cttgtgtgca gcacctggag ggaaaacaac acacattgca 1200 gcactaatgc atgatcaggg agaagttata gcactggata aaatcttcaa caaagtagaa 1260 aaaatcaaac agaatgcctt attgttaggg ctgaattcca tcagggcatt ttgttttgat 1320 ggaacaaagg cggttaaact tgatatggtg gaggacacag aaggagaacc tccatttcta 1380 ccagaatcct ttgaccgaat tcttctggat gcaccctgta gtggaatggg acagagacca 1440 aacatggcct gtacttggtc tgtgaaggaa gtggcatcat atcagccatt acagcgaaaa 1500 ctcttcactg cagcggttca gctgctgaag ccagagggtg tgctggttta tagcacgtgc 1560 actataacac tggccgaaaa tgaagaacag gttgcctggg ccctgacaaa atttccttgc 1620 cttcagcttc agccccagga accgcagatt ggaggagaag gaatgagggg agctgggctc 1680 tcatgtgaac agttgaaaca gctgcagcga tttgatccat cggctgtgcc attaccggac 1740 actgacatgg actctcttag agaggccaga agagaagaca tgttgcgtct ggctaataag 1800 gactctatag gtttttttat tgcaaaattt gtaaaatgca aaagcacata ggagagggat 1860 ggatgctcag aaatgaaaat tccaaacatt tgctgtctgt ggtttttttt tttttttttt 1920 taaccaaagt gttgtcaggc caactgaatg atgatgtggt tgctatggaa acagaaaagg 1980 ctgccagctg ttttaccagg gatccagaga catagaggaa gtagggggtg gtatgagatt 2040 atattttctg tttttaaaag attttttttt tttatgtatt tagtagagta taaagaaaag 2100 cagatgccta tagatgtctg gagcatattt tcatttgtga tctaatgttt taatttgtaa 2160 agtgtacaag tcatttttaa tgttaaaaat tagtgaatct aacaaaagga ataaattagc 2220 aatatt 2226 91 2362 DNA Homo sapiens misc_feature Incyte ID No 5584860CB1 91 cccgggtcga cccacgcgtc cgaaataaga cgccgaccgg cgcggcgcta gcctcggggc 60 ttgacgggat tgtggcggtc ctctctccca attcggaagc tacagctacc tccggacgct 120 ctcaagatgg cgacctctct gggttccaac acctacaaca ggcagaactg ggaggatgcg 180 gacttcccca ttctgtgcca gacatgtctt ggagaaaacc catatatccg aatgaccaaa 240 gaaaagtatg ggaaggaatg caaaatctgt gccaggccat tcacagtgtt tcgctggtgc 300 cctggagtcc gcatgcgttt caagaagact gaagtgtgcc aaacctgcag taaattgaag 360 aatgtctgtc agacctgcct cttagaccta gagtatggcc tgcccatcca ggttcgtgac 420 gcaggattgt cttttaaaga tgacatgcca aagtcagatg tcaacaaaga gtactataca 480 cagaatatgg agagagagat ttctaactct gatggaacac ggccagttgg catgctgggg 540 aaagccacat ctaccagtga catgctgctc aaactggccc ggaccacacc ctactacaaa 600 aggaatcgac cccacatttg ctccttctgg gtgaaaggag agtgtaagag aggagaggaa 660 tgtccataca gacatgagaa gcctacagat ccagatgacc cccttgctga tcagaatatt 720 aaagaccgtt attacggaat caatgatcct gtagctgaca agcttctaaa gcgggcttca 780 acaatgcctc ggctggaccc accagaggat aaaactatca ccacactata tgttggtggt 840 ctaggtgata ccattactga gacagattta agaaatcatt tctaccagtt cggagagatc 900 cggacgatca ctgttgtgca gagacagcag tgtgctttca tccagtttgc cacacggcag 960 gctgcagaag tggctgctga gaagtccttt aataagttga ttgtaaatgg ccgcagactg 1020 aatgtgaaat ggggaagatc ccaggcagcc agaggaaaag aaaaagagaa agatggaact 1080 acagactctg ggatcaaact agaacctgtt ccaggattgc caggagctct tcctcctcct 1140 cctgcagcag aagaagaagc ctctgccaac tacttcaact tgcccccaag tggtcctcca 1200 gctgtggtga acattgctct gccaccgccc cctggcattg ctccaccccc acccccaggt 1260 tttgggccac acatgttcca cccaatggga ccaccccctc ctttcatgcg ggctccagga 1320 ccaatccact atccttctca ggaccctcag aggatgggag ctcatgctgg aaaacacagc 1380 agcccctagc accttgtcac cactctgggg ctctgtggaa gaaagggcac ttaaaactcc 1440 cagtaaatct tggaataaat atatttttcc ttcccttgta gtttccatgg tagctgaatg 1500 tgctcagatg tgagcagtca gagactgaca gccatgcttt cctatacttg ttcaaaggat 1560 cgatggaccg taaataagct gccattaaca catctggtta ctgctgtaac atgactaata 1620 aaaccgaacg cctgttcccc ttacccgtgt gggggacacg cagatgagtg aattggaatg 1680 tccagcagag ttaccctccc aattatatgt tcattttgta tattttttgg tcgggggaaa 1740 aattgacctg cagtaaaaaa acctttgacc atttttatgt ccattggata ctttcctttt 1800 tatcatctta aaaaaagata actagtacta atcattgtag tggcctaagt gtgatttaac 1860 tcttgaagtc acaccctccg aaagatgagt agaaaccagc accagcacag cccagatctt 1920 ctctttcctc tccttttcct catttattcc taaaggaatc tgaccatttt acgtctctac 1980 ggcccaaaaa aagacaaaaa taaaaattcc tttttattcc tgtcaactgg atggaaacac 2040 aaatttcatg gagctgtgta ccatcgaaga aacctggtgt ctggcatgaa attactgtaa 2100 agaacttcct gtaaaacacg ttctttaaca aactgaaatg aaaagcattg gagcgtctga 2160 atgaaagacg tgacctcctg ctgggactct gatggtcttc agcattcacc ttcgtgtgtc 2220 ttcagtgtct cattgtcatc cctgcttctg tttggtctta gagtgtttgg atataactga 2280 attgtagatg gtaaaggaaa tttgatgtgt tttttgtttt taaataatta aaacgggtca 2340 atttttcaaa aaaaaaaaaa aa 2362 92 731 DNA Homo sapiens misc_feature Incyte ID No 5807892CB1 92 tagggcggca agcggaggag gcgtggcgag cggatcatcc gcttccggag tcgaggtttt 60 cgggcttgta ccgcttggcg gtgcggcctg gtgtcggctt gcaggttctt tctgtgtttg 120 ttctctgccc tgccaaggcc gtagagctgg tgcgtgcggg tagcggggct ctccgaggag 180 ccgcacgccg gcggcaccat ggtccacctc actactctcc tctgcaaggc ctaccgtggg 240 ggccacttaa ccatccgcct tgccctgggt ggctgcacca atcggccgtt ctaccgcatt 300 gtggctgctc acaacaagtg tcccagggat ggccgtttcg tagagcagct gggctcctat 360 gatccattgc ccaacagtca tggagaaaaa ctcgttgccc tcaacctaga caggatccgt 420 cattggattg gctgcggggc ccacctctct aagcctatgg aaaagcttct gggtcttgct 480 ggctttttcc ctctgcatcc tatgatgatc acaaatgctg agagactgcg aaggaaacgg 540 gcacgtgaag tcctgttagc ttctcagaaa acagatgcag aagctacaga tacagaggct 600 acagaaacat aaatgagctg actttagtga gcatagcagt gggaacaagg tcaaggtcct 660 tttgaaacac tgcagcgatc ttaattttgt tagatttgga gttcaataaa tggagtatcc 720 tgaaaaaaaa a 731 93 2088 DNA Homo sapiens misc_feature Incyte ID No 3210044CB1 93 ctttccagaa aatcaaatga aagattcaga gtatattcat gaattaattt tttttcaaaa 60 ccctaaattt aatcagctgg aattacttta aaagtgtcat tctatttaac ttttgggaat 120 gatgaatttg ccttttaata gggatgctgt attttatcat gaagatgaaa caaactgtct 180 tttgttaatt atggcacctt catttaccgc ccgcattcag ttgttcctct tgcgggcgct 240 aggctttctc ataggcttag taggccgagc agctttagtc ttagggggcc caaagtttgc 300 ctcaaagacc cctcggccgg tgactgaacc attgcttctg ctttcgggga tgcagctggc 360 caagctgatc cgacagagaa aggtgaaatg tatagatgtt gttcaggctt atatcaacag 420 aatcaaggac gtgaacccaa tgatcaatgg aattgtcaag tacaggtttg aggaagcgat 480 gaaggaggct catgctgtag atcaaaagct tgcagagaag caggaagatg aagccaccct 540 ggaaaataaa tggcccttcc ttggggttcc tttgacagtc aaggaagctt tccagctaca 600 aggaatgccc aattcttctg gactcatgaa ccgtcgtgat gccattgcca aaacagatgc 660 cactgtggtg gcattactga agggagctgg tgccattcct cttggcataa ccaactgtag 720 tgagttgtgt atgtggtatg aatccagtaa caagatctat ggccgatcaa acaacccata 780 tgatttacag catattgtag gtggaagttc tggtggtgag ggctgcacac tggcagctgc 840 ctgctcagtt attggtgtgg gctctgatat tggtggtagc attcgaatgc ctgctttctt 900 caatggtata tttggacaca agccttctcc aggtgtggtt cccaacaaag gtcagtttcc 960 cttggctgtg ggagcccagg agttgtttct gtgcactggt cctatgtgcc gctatgctga 1020 agacctggcc cccatgttga aggtcatggc aggacctggg atcaaaaggt taaaactaga 1080 cacaaaggta catttaaaag acttaaaatt ttactggatg gaacatgatg gaggctcatt 1140 tttaatgtcc aaagtggacc aagatctcat tatgactcag aaaaaggttg tggttcacct 1200 tgaaactatt ctaggagcct cagttcaaca tgttaaactg aagaaaatga agtactcttt 1260 tcagttgtgg atcgcaatga tgtcagcaaa gggacatgat gggaaggaac ctgtgaaatt 1320 tgtagatttg cttggtgacc atgggaaaca tgtcagtcct ctgtgggagt tgatcaaatg 1380 gtgcctgggt ctgtcagtgt acaccatccc ttccattgga ctggctttgt tggaagaaaa 1440 gctcagatat agcaatgaga aataccaaaa gtttaaggca gtggaagaaa gcctgcgtaa 1500 agagctggtg gatatgctag gtgatgatgg tgtgttctta tatccctcac atcccacagt 1560 ggcacctaag catcatgtcc ctctaacacg gcctttcaac tttgcttaca caggtgtctt 1620 cagtgccctg ggtttgcctg tgacccaatg cccactggga ctgaatgcca aaggactccc 1680 tttaggcatc caggttgtgg ctggaccctt taatgatcat ctgaccctgg ctgtggccca 1740 gtacttggag aaaacttttg ggggctgggt ctgtccagga aagttttagg aggaccttct 1800 gcaaggttaa tgtgtgtgtg tgtttgtgtt cgtgtggtgg tgtttctatt aattgggtga 1860 aatcaagcac cagcagacaa gcagagaaac aactggggaa tttattgact catttagtta 1920 ttctttctac ttttatttcc ttctctaact gttggtctta ctaaaatggt aatatttgct 1980 tcttgctttt atgttactgg aaaattagga catgtaaatg gataagtgca ataaagtttc 2040 ctaaatgctg aaaaaaaaaa acacaaaaaa aacaaaaaaa aaaaaaaa 2088 94 660 DNA Homo sapiens misc_feature Incyte ID No 4942454CB1 94 ccgtcaatag cctccgcctc tccttccagt gtccgccgtc gtgcgctcgc tacccctctc 60 cctcgaggcc tttgccggcg aagagcgccc agtcgcccac caggatgaag tttgttgctg 120 cctacctgct tgctgtcctc gctgggaact ccagcccctc tgccgaggac ttgacagcca 180 ttctggagtc agttggctgt gaagttgaca atgaaaagat ggaactcctt ctgtcccaac 240 tgagcggtaa ggacattacc gagctcattg ctgctggcag ggagaagttt gcttcagtcc 300 catgtggcgg tggcggtgtg gctgttgcgg cagctgcccc tgctgctggc ggcgctcctg 360 cagctgaggc gaagaaagaa gagaaggtgg aggagaagga agaaagtgat gacgacatgg 420 gcttcagcct cttcgactaa gcctgtgcaa tagtcaagag tattgttttt gagtcgcgga 480 agcagaggga agaaaaatcg tagtcatgtt tggactttaa ctttgtttta tgttggaaag 540 tacttgaaag acttttcctg tggtaattct aggcgtaggt tgctgtgctg gttggggttt 600 actggtgaac cagagttttt ctatctccca ctatgaattt gttacctcaa gttacctgtg 660 

What is claimed is:
 1. An isolated polypeptide selected from the group consisting of: a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, b) a naturally occurring polypeptide comprising an amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47.
 2. An isolated polypeptide of claim 1 selected from the group consisting of SEQ ID NO:1-47.
 3. An isolated polynucleotide encoding a polypeptide of claim
 1. 4. An isolated polynucleotide encoding a polypeptide of claim
 2. 5. An isolated polynucleotide of claim 4 selected from the group consisting of SEQ ID NO:48-94.
 6. A recombinant polynucleotide comprising a promoter sequence operably linked to a polynucleotide of claim
 3. 7. A cell transformed with a recombinant polynucleotide of claim
 6. 8. A transgenic organism comprising a recombinant polynucleotide of claim
 6. 9. A method for producing a polypeptide of claim 1, the method comprising: a) culturing a cell under conditions suitable for expression of the polypeptide, wherein said cell is transformed with a recombinant polynucleotide, and said recombinant polynucleotide comprises a promoter sequence operably linked to a polynucleotide encoding the polypeptide of claim 1, and b) recovering the polypeptide so expressed.
 10. An isolated antibody which specifically binds to a polypeptide of claim
 1. 11. An isolated polynucleotide selected from the group consisting of: a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:48-94, b) a naturally occurring polynucleotide comprising a polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:48-94, c) a polynucleotide complementary to a polynucleotide of a), d) a polynucleotide complementary to a polynucleotide of b), and e) an RNA equivalent of a)-d).
 12. An isolated polynucleotide comprising at least 60 contiguous nucleotides of a polynucleotide of claim
 11. 13. A method for detecting a target polynucleotide in a sample, said target polynucleotide having a sequence of a polynucleotide of claim 11, the method comprising: a) hybridizing the sample with a probe comprising at least 20 contiguous nucleotides comprising a sequence complementary to said target polynucleotide in the sample, and which probe specifically hybridizes to said target polynucleotide, under conditions whereby a hybridization complex is formed between said probe and said target polynucleotide or fragments thereof, and b) detecting the presence or absence of said hybridization complex, and, optionally, if present, the amount thereof.
 14. A method of claim 13, wherein the probe comprises at least 60 contiguous nucleotides.
 15. A method for detecting a target polynucleotide in a sample, said target polynucleotide having a sequence of a polynucleotide of claim 11, the method comprising: a) amplifying said target polynucleotide or fragment thereof using polymerase chain reaction amplification, and b) detecting the presence or absence of said amplified target polynucleotide or fragment thereof, and, optionally, if present, the amount thereof.
 16. A composition comprising a polypeptide of claim 1 and a pharmaceutically acceptable excipient.
 17. A composition of claim 16, wherein the polypeptide has an amino acid sequence selected from the group consisting of SEQ ID NO:1-47.
 18. A method for treating a disease or condition associated with decreased expression of functional RMEP, comprising administering to a patient in need of such treatment the composition of claim
 16. 19. A method for screening a compound for effectiveness as an agonist of a polypeptide of claim 1, the method comprising: a) exposing a sample comprising a polypeptide of claim 1 to a compound, and b) detecting agonist activity in the sample.
 20. A composition comprising an agonist compound identified by a method of claim 19 and a pharmaceutically acceptable excipient.
 21. A method for treating a disease or condition associated with decreased expression of functional RMEP, comprising administering to a patient in need of such treatment a composition of claim
 20. 22. A method for screening a compound for effectiveness as an antagonist of a polypeptide of claim 1, the method comprising: a) exposing a sample comprising a polypeptide of claim 1 to a compound, and b) detecting antagonist activity in the sample.
 23. A composition comprising an antagonist compound identified by a method of claim 22 and a pharmaceutically acceptable excipient.
 24. A method for treating a disease or condition associated with overexpression of functional RMEP, comprising administering to a patient in need of such treatment a composition of claim
 23. 25. A method of screening for a compound that specifically binds to the polypeptide of claim 1, said method comprising the steps of: a) combining the polypeptide of claim 1 with at least one test compound under suitable conditions, and b) detecting binding of the polypeptide of claim 1 to the test compound, thereby identifying a compound that specifically binds to the polypeptide of claim
 1. 26. A method of screening for a compound that modulates the activity of the polypeptide of claim 1, said method comprising: a) combining the polypeptide of claim 1 with at least one test compound under conditions permissive for the activity of the polypeptide of claim 1, b) assessing the activity of the polypeptide of claim 1 in the presence of the test compound, and c) comparing the activity of the polypeptide of claim 1 in the presence of the test compound with the activity of the polypeptide of claim 1 in the absence of the test compound, wherein a change in the activity of the polypeptide of claim 1 in the presence of the test compound is indicative of a compound that modulates the activity of the polypeptide of claim
 1. 27. A method for screening a compound for effectiveness in altering expression of a target polynucleotide, wherein said target polynucleotide comprises a sequence of claim 5, the method comprising: a) exposing a sample comprising the target polynucleotide to a compound, under conditions suitable for the expression of the target polynucleotide, b) detecting altered expression of the target polynucleotide, and c) comparing the expression of the target polynucleotide in the presence of varying amounts of the compound and in the absence of the compound.
 28. A method for assessing toxicity of a test compound, said method comprising: a) treating a biological sample containing nucleic acids with the test compound; b) hybridizing the nucleic acids of the treated biological sample with a probe comprising at least 20 contiguous nucleotides of a polynucleotide of claim 11 under conditions whereby a specific hybridization complex is formed between said probe and a target polynucleotide in the biological sample, said target polynucleotide comprising a polynucleotide sequence of a polynucleotide of claim 11 or fragment thereof; c) quantifying the amount of hybridization complex; and d) comparing the amount of hybridization complex in the treated biological sample with the amount of hybridization complex in an untreated biological sample, wherein a difference in the amount of hybridization complex in the treated biological sample is indicative of toxicity of the test compound.
 29. A diagnostic test for a condition or disease associated with the expression of RMEP in a biological sample comprising the steps of: a) combining the biological sample with an antibody of claim 10, under conditions suitable for the antibody to bind the polypeptide and form an antibody:polypeptide complex; and b) detecting the complex, wherein the presence of the complex correlates with the presence of the polypeptide in the biological sample.
 30. The antibody of claim 10, wherein the antibody is: a) a chimeric antibody, b) a single chain antibody, c) a Fab fragment, d) a F(ab′)₂ fragment, or e) a humanized antibody.
 31. A composition comprising an antibody of claim 10 and an acceptable excipient.
 32. A method of diagnosing a condition or disease associated with the expression of RMEP in a subject, comprising administering to said subject an effective amount of the composition of claim
 31. 33. A composition of claim 31, wherein the antibody is labeled.
 34. A method of diagnosing a condition or disease associated with the expression of RMEP in a subject, comprising administering to said subject an effective amount of the composition of claim
 33. 35. A method of preparing a polyclonal antibody with the specificity of the antibody of claim 10 comprising: a) immunizing an animal with a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, or an immunogenic fragment thereof, under conditions to elicit an antibody response; b) isolating antibodies from said animal; and c) screening the isolated antibodies with the polypeptide, thereby identifying a polyclonal antibody which binds specifically to a polypeptide having an ammo acid sequence selected from the group consisting of SEQ ID NO:1-47.
 36. An antibody produced by a method of claim
 35. 37. A composition comprising the antibody of claim 36 and a suitable carrier.
 38. A method of making a monoclonal antibody with the specificity of the antibody of claim 10 comprising: a) immunizing an animal with a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47, or an immunogenic fragment thereof, under conditions to elicit an antibody response; b) isolating antibody producing cells from the animal; c) fusing the antibody producing cells with immortalized cells to form monoclonal antibody-producing hybridoma cells; d) culturing the hybridoma cells; and e) isolating from the culture monoclonal antibody which binds specifically to a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47.
 39. A monoclonal antibody produced by a method of claim
 38. 40. A composition comprising the antibody of claim 39 and a suitable carrier.
 41. The antibody of claim 10, wherein the antibody is produced by screening a Fab expression library.
 42. The antibody of claim 10, wherein the antibody is produced by screening a recombinant immunoglobulin library.
 43. A method for detecting a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47 in a sample, comprising the steps of: a) incubating the antibody of claim 10 with a sample under conditions to allow specific binding of the antibody and the polypeptide; and b) detecting specific binding, wherein specific binding indicates the presence of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47 in the sample.
 44. A method of purifying a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47 from a sample, the method comprising: a) incubating the antibody of claim 10 with a sample under conditions to allow specific binding of the antibody and the polypeptide; and b) separating the antibody from the sample and obtaining the purified polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-47.
 45. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:1.
 46. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:2.
 47. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:3.
 48. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:4.
 49. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:5.
 50. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:6.
 51. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:7.
 52. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:8.
 53. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:9.
 54. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:10.
 55. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:11.
 56. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:12.
 57. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:13.
 58. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:14.
 59. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:15.
 60. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:16.
 61. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:17.
 62. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:18.
 63. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:19.
 64. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:20.
 65. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:21.
 66. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:22.
 67. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:23.
 68. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:24.
 69. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:25.
 70. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:26.
 71. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:27.
 72. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:28.
 73. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:29.
 74. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:30.
 75. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:31.
 76. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:32.
 77. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:33.
 78. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:34.
 79. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO;35.
 80. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:36.
 81. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:37.
 82. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:38.
 83. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:39.
 84. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:40.
 85. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:41.
 86. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:42.
 87. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:43.
 88. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:44.
 89. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:45.
 90. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:46.
 91. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:47.
 92. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:48.
 93. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:49.
 94. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:50.
 95. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:51.
 96. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:52.
 97. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:53.
 98. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:54.
 99. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:55.
 100. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:56.
 101. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:57.
 102. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:58.
 103. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:59.
 104. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:60.
 105. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:61.
 106. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:62.
 107. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:63.
 108. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:64.
 109. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:65.
 110. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:66.
 111. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:67.
 112. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:68.
 113. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:69.
 114. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:70.
 115. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:71.
 116. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:72.
 117. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:73.
 118. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:74.
 119. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:75.
 120. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:76.
 121. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:77.
 122. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:78.
 123. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:79.
 124. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:80.
 125. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:81.
 126. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:82.
 127. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:83.
 128. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:84.
 129. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:85.
 130. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:86.
 131. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:87.
 132. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:88.
 133. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:89.
 134. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:90.
 135. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:91.
 136. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:92.
 137. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:93.
 138. A polynucleotide of claim 11, comprising the polynucleotide sequence of SEQ ID NO:94.
 139. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:1.
 140. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:2.
 141. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:3.
 142. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:4.
 143. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:5.
 144. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:6.
 145. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:7.
 146. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:8.
 147. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:9.
 148. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:10.
 149. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:11.
 150. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:12.
 151. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:13.
 152. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:14.
 153. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:15.
 154. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:16.
 155. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:17.
 156. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:18.
 157. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:19.
 158. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:20.
 159. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:21.
 160. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:22.
 161. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:23.
 162. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:24.
 163. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:25.
 164. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:26.
 165. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:27.
 166. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:28.
 167. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:29.
 168. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:30.
 169. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:31.
 170. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:32.
 171. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:33.
 172. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:34.
 173. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:35.
 174. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:36.
 175. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:37.
 176. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:38.
 177. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:39.
 178. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:40.
 179. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:41.
 180. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:42.
 181. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:43.
 182. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:44.
 183. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:45.
 184. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:46.
 185. A method of claim 9, wherein the polypeptide has the sequence of SEQ ID NO:47.
 186. A microarray wherein at least one element of the microarray is a polynucleotide of claim
 12. 187. A method for generating a transcript image of a sample which contains polynucleotides, the method comprising the steps of: a) labeling the polynucleotides of the sample, b) contacting the elements of the microarray of claim 186 with the labeled polynucleotides of the sample under conditions suitable for the formation of a hybridization complex, and c) quantifying the expression of the polynucleotides in the sample.
 188. An array comprising different nucleotide molecules affixed in distinct physical locations on a solid substrate, wherein at least one of said nucleotide molecules comprises a first oligonucleotide or polynucleotide sequence specifically hybridizable with at least 30 contiguous nucleotides of a target polynucleotide, said target polynucleotide having a sequence of claim
 11. 189. An array of claim 188, wherein said first oligonucleotide or polynucleotide sequence is completely complementary to at least 30 contiguous nucleotides of said target polynucleotide.
 190. An array of claim 188, wherein said first oligonucleotide or polynucleotide sequence is completely complementary to at least 60 contiguous nucleotides of said target polynucleotide.
 191. An array of claim 188, which is a microarray.
 192. An array of claim 188, further comprising said target polynucleotide hybridized to said first oligonucleotide or polynucleotide.
 193. An array of claim 188, wherein a linker joins at least one of said nucleotide molecules to said solid substrate.
 194. An array of claim 188, wherein each distinct physical location on the substrate contains multiple nucleotide molecules having the same sequence, and each distinct physical location on the substrate contains nucleotide molecules having a sequence which differs from the sequence of nucleotide molecules at another physical location on the substrate. 